Canonical Allele Identifier: PA2573192111
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1352610
ClinVar RCV Id: RCV002039818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Ala952Ser
CA393851021
NM_001287248.2:c.2854G>T