Canonical Allele Identifier: PA658679955
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455330
ClinVar RCV Id: RCV000546866
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu17Pro
CA346734547
NM_000179.3:c.50T>C