Canonical Allele Identifier: PA2826739764
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2452533
ClinVar RCV Id: RCV003177307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.His1019Tyr
CA274767360
NM_001287247.2:c.3055C>T