Canonical Allele Identifier: PA916016319
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 524798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Tyr995His
CA274764723
NM_001287247.2:c.2983T>C