Allele Registry

Canonical Allele Identifier: PA2825041513

Gene: BLM HGNC NCBI

ClinVar RCV:

RCV002326040

ClinVar Variation:

1727700

HGVS (amino-acid)	Matching Registered Transcripts
NP_000048.1:p.Cys1036Tyr	CA393846850 NM_000057.4:c.3107G>A