Canonical Allele Identifier: PA2826738863
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 128530
ClinVar RCV Id: RCV000116501 RCV000281046 RCV000566425 RCV001530630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Val1321Ile
CA152047
NM_001287246.2:c.3961G>A