Canonical Allele Identifier: PA2826629524
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766466
ClinVar RCV Id: RCV002371507
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu8Pro
CA073592
NM_001281493.2:c.23T>C