Canonical Allele Identifier: PA2826633308
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly884Asp
CA013435
NM_001281493.2:c.2651G>A