Canonical Allele Identifier: PA2826738811
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1735916
ClinVar RCV Id: RCV002357418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Gly1298Glu
CA393850440
NM_001287246.2:c.3893G>A