Canonical Allele Identifier: PA2826631460
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp461Gly
CA16610931
NM_001281493.2:c.1382A>G