Canonical Allele Identifier: PA2826740198
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1737523
ClinVar RCV Id: RCV002321442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Ala1226Ser
CA393851556
NM_001287247.2:c.3676G>T