Canonical Allele Identifier: PA2826630824
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182628
ClinVar RCV Id: RCV000160673 RCV000212653 RCV000410091 RCV000304378 RCV000524120 RCV001193697 RCV001798554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys313Ser
CA009314
NM_001281493.2:c.938G>C
CA346749634
NM_001281493.2:c.937T>A