Canonical Allele Identifier: PA2826629201
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro1179Leu
CA346761473
NM_001281492.2:c.3536C>T