Canonical Allele Identifier: PA916010963
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 449945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala34Thr
CA346734831
NM_001281492.2:c.100G>A