Allele Registry

Canonical Allele Identifier: PA2825316653

Gene: BCAM HGNC NCBI

ClinVar RCV:

RCV000000468

RCV002496219

RCV003964784

ClinVar Variation:

439

HGVS (amino-acid)	Matching Registered Transcripts
NP_001013275.1:p.Thr539Ala	CA114286 NM_001013257.2:c.1615A>G