Allele Registry

Canonical Allele Identifier: PA916016641

Gene: BLM HGNC NCBI

ClinVar Variation Id: 180588

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274177.1:p.Glu942Lys	CA273735 NM_001287248.2:c.2824G>A