Canonical Allele Identifier: PA337354
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216307
ClinVar RCV Id: RCV001190573 RCV001313045 RCV003454503
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu773Pro
CA337352
NM_000179.3:c.2318T>C