Canonical Allele Identifier: PA915964428
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys606Arg
CA346749430
NM_000179.3:c.1817A>G