Canonical Allele Identifier: PA2826633521
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val930Asp
CA013875
NM_001281493.2:c.2789T>A