Canonical Allele Identifier: PA2826738157
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 524798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Tyr995His
CA274764723
NM_001287246.2:c.2983T>C