Canonical Allele Identifier: PA2825088074
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773637
ClinVar RCV Id: RCV003584493
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala440Thr
CA346744417
NM_000179.3:c.1318G>A