Canonical Allele Identifier: PA658801982
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525651
ClinVar RCV Id: RCV000629798 RCV002377345 RCV002305519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala297Val
CA346740686
NM_000179.3:c.890C>T