Canonical Allele Identifier: PA2826739790
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1523874
ClinVar RCV Id: RCV002031296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Glu1031Gly
CA393846816
NM_001287247.2:c.3092A>G