Canonical Allele Identifier: PA332772
Gene: EPCAM HGNC NCBI

Linked Data

ClinVar Variation Id: 136020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002345.2:p.Ala107Thr
CA332770
NM_002354.3:c.319G>A