Canonical Allele Identifier: PA2741856022
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2698760
ClinVar RCV Id: RCV003505509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Glu642Gln
CA393846713
NM_001287248.2:c.1924G>C