Canonical Allele Identifier: PA2573163513
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala704Gly
CA068474
NM_000179.3:c.2111C>G