Allele Registry

Canonical Allele Identifier: PA2826738488

Gene: BLM HGNC NCBI

ClinVar RCV:

RCV000475513

RCV000708668

ClinVar Variation:

405312

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274175.1:p.Arg1139Pro	CA7739029 NM_001287246.2:c.3416G>C