Canonical Allele Identifier: PA916015687
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 133708
ClinVar RCV Id: RCV000120237 RCV000224918 RCV000234547 RCV000570211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Glu140Gly
CA157415
NM_001287247.2:c.419A>G