Canonical Allele Identifier: PA2826635743
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala402Gly
CA068474
NM_001281494.2:c.1205C>G