Allele Registry

Canonical Allele Identifier: PA100955

Gene: BCO1 HGNC NCBI

ClinVar RCV:

RCV000005038

RCV002247250

RCV003924801

ClinVar Variation:

4772

HGVS (amino-acid)	Matching Registered Transcripts
NP_059125.2:p.Thr170Met	CA117066 NM_017429.3:c.509C>T