Canonical Allele Identifier: PA2826738150
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 822402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Phe992Ser
CA274764721
NM_001287246.2:c.2975T>C