Canonical Allele Identifier: PA2825092637
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736069
ClinVar RCV Id: RCV002357491
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1303Thr
CA46719773
NM_000179.3:c.3907G>A