Canonical Allele Identifier: PA2826630242
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772651
ClinVar RCV Id: RCV002394307
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val178Ile
CA346745593
NM_001281493.2:c.532G>A