Canonical Allele Identifier: PA2825092307
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His1266Asp
CA346761188
NM_000179.3:c.3796C>G