Canonical Allele Identifier: PA658680931
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479919
ClinVar RCV Id: RCV000562492 RCV000629918
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys771Thr
CA346753136
NM_000179.3:c.2312A>C