Canonical Allele Identifier: PA2826627293
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038121
ClinVar RCV Id: RCV001341390 RCV002447401
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile675Thr
CA346753995
NM_001281492.2:c.2024T>C