Canonical Allele Identifier: PA658673989
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 460561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005350.1:p.Asn213Ser
CA8965840
NM_005359.6:c.638A>G