Allele Registry

Canonical Allele Identifier: PA2826738800

Gene: BLM HGNC NCBI

ClinVar Variation Id: 701143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274175.1:p.Glu1293Gly	CA7739152 NM_001287246.2:c.3878A>G