Allele Registry

Canonical Allele Identifier: PA2825041211

Gene: BLM HGNC NCBI

ClinVar RCV:

RCV001061142

ClinVar Variation:

855803

HGVS (amino-acid)	Matching Registered Transcripts
NP_000048.1:p.Pro868Gln	CA393845693 NM_000057.4:c.2603C>A