Allele Registry

Canonical Allele Identifier: PA2826736010

Gene: BLM HGNC NCBI

ClinVar RCV:

RCV000227410

RCV000572998

RCV000857675

RCV003226261

RCV003407767

ClinVar Variation:

236821

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274175.1:p.Arg15Cys	CA7738228 NM_001287246.2:c.43C>T