Canonical Allele Identifier: PA2580264819
Gene: EPCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 1747779
ClinVar RCV Id: RCV002349831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002345.2:p.Ser183Cys
CA346724056
NM_002354.3:c.547A>T