Canonical Allele Identifier: PA645381108
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu638del
CA16611140
NM_000179.3:c.1912_1914del