Allele Registry

Canonical Allele Identifier: PA2826740393

Gene: BLM HGNC NCBI

ClinVar RCV:

RCV000562284

RCV001313055

ClinVar Variation:

485353

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274177.1:p.Gln28His	CA393842555 NM_001287248.2:c.84G>C CA393842556 NM_001287248.2:c.84G>T