Canonical Allele Identifier: PA2826627203
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys653Ser
CA068851
NM_001281492.2:c.1957T>A
CA346753511
NM_001281492.2:c.1958G>C