Canonical Allele Identifier: PA2741855661
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2586889
ClinVar RCV Id: RCV003341928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Glu332Ala
CA393842056
NM_001287247.2:c.995A>C