Canonical Allele Identifier: PA916016425
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 485362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Thr659Met
CA7738939
NM_001287248.2:c.1976C>T