Canonical Allele Identifier: PA2826740997
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1787797
ClinVar RCV Id: RCV002425894 RCV003098718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Thr363Ile
CA393844803
NM_001287248.2:c.1088C>T