Canonical Allele Identifier: PA2826626425
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075076
ClinVar RCV Id: RCV004015602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu474Ala
CA346749388
NM_001281492.2:c.1421A>C