Allele Registry

Canonical Allele Identifier: PA2826740068

Gene: BLM HGNC NCBI

ClinVar Variation Id: 701143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274176.1:p.Glu1162Gly	CA7739152 NM_001287247.2:c.3485A>G