Canonical Allele Identifier: PA645381085
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233917
ClinVar RCV Id: RCV000217487 RCV000464191 RCV000480702 RCV001293521 RCV003998588
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly624Val
CA068227
NM_000179.3:c.1871G>T