Canonical Allele Identifier: PA2826738828
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1481760
ClinVar RCV Id: RCV002025013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Gly1306Asp
CA393850600
NM_001287246.2:c.3917G>A