Canonical Allele Identifier: PA645382017
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys783Ser
CA068851
NM_000179.3:c.2347T>A
CA346753511
NM_000179.3:c.2348G>C