Allele Registry

Canonical Allele Identifier: PA287879

Gene: EPCAM HGNC NCBI

ClinVar RCV:

RCV000115770

RCV000123185

RCV000589651

RCV000664266

ClinVar Variation:

127848

HGVS (amino-acid)	Matching Registered Transcripts
NP_002345.2:p.Gln89His	CA287877 NM_002354.3:c.267G>C CA346722988 NM_002354.3:c.267G>T