Canonical Allele Identifier: PA2826631304
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly421Arg
CA16617669
NM_001281493.2:c.1261G>C