Canonical Allele Identifier: PA658681390
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479908
ClinVar RCV Id: RCV000571415 RCV001858109
ClinVar Variation Id: 1501725
ClinVar RCV Id: RCV002010790 RCV002458972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1217Ser
CA346760817
NM_000179.3:c.3651A>C
CA346760818
NM_000179.3:c.3651A>T