Canonical Allele Identifier: PA2826739798
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 967424
ClinVar RCV Id: RCV001242329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Thr1034Lys
CA393846837
NM_001287247.2:c.3101C>A