Canonical Allele Identifier: PA2826625782
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 571875
ClinVar RCV Id: RCV000693125 RCV001187695
ClinVar Variation Id: 818962
ClinVar RCV Id: RCV001011091
ClinVar Variation Id: 2869887
ClinVar RCV Id: RCV003759433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe321Leu
CA346744665
NM_001281492.2:c.961T>C
CA346744681
NM_001281492.2:c.963C>A
CA346744688
NM_001281492.2:c.963C>G