Canonical Allele Identifier: PA299457
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182634
ClinVar RCV Id: RCV000160679 RCV000821022 RCV000772630 RCV003998496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr754Pro
CA009921
NM_000179.3:c.2260A>C