Canonical Allele Identifier: PA2825089282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2061803
ClinVar RCV Id: RCV002939135
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly723Ser
CA346751162
NM_000179.3:c.2167G>A