Canonical Allele Identifier: PA658681491
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1302Thr
CA346761429
NM_000179.3:c.3904G>A