Canonical Allele Identifier: PA2580197090
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1727522
ClinVar RCV Id: RCV002325862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Ile658Val
CA393846829
NM_001287248.2:c.1972A>G