Canonical Allele Identifier: PA2580264818
Gene: EPCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 1747656
ClinVar RCV Id: RCV002349708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002345.2:p.Thr182Met
CA346724053
NM_002354.3:c.545C>T