Canonical Allele Identifier: PA2825042006
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1481760
ClinVar RCV Id: RCV002025013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000048.1:p.Gly1306Asp
CA393850600
NM_000057.4:c.3917G>A