Canonical Allele Identifier: PA2826634245
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229741
ClinVar RCV Id: RCV000219163 RCV000475100 RCV000478810 RCV000659889 RCV000761132 RCV002265689
ClinVar Variation Id: 649649
ClinVar RCV Id: RCV000804626
ClinVar Variation Id: 2842405
ClinVar RCV Id: RCV003758465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser12Arg
CA073603
NM_001281494.2:c.36C>G
CA346740775
NM_001281494.2:c.34A>C
CA346740781
NM_001281494.2:c.36C>A