Canonical Allele Identifier: PA2825087213
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769302
ClinVar RCV Id: RCV003594541
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val296Leu
CA346740677
NM_000179.3:c.886G>C