Canonical Allele Identifier: PA916010964
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala34Val
CA067035
NM_001281492.2:c.101C>T