Canonical Allele Identifier: PA1139690927
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_001274177.1:p.Thr659Lys
CA393846837
NM_001287248.2:c.1976C>A