Canonical Allele Identifier: PA2826628594
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 846478
ClinVar RCV Id: RCV001049789
ClinVar Variation Id: 2986028
ClinVar RCV Id: RCV003843699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser1058Arg
CA346760433
NM_001281492.2:c.3172A>C
CA346760442
NM_001281492.2:c.3174T>A
CA346760444
NM_001281492.2:c.3174T>G