Canonical Allele Identifier: PA916016657
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 824520
ClinVar RCV Id: RCV001021698 RCV001313764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Ser967Pro
CA393851316
NM_001287248.2:c.2899T>C