Canonical Allele Identifier: PA2825092609
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587370
ClinVar RCV Id: RCV003360839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe1300Tyr
CA346761418
NM_000179.3:c.3899T>A