Canonical Allele Identifier: PA2741856042
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2586871
ClinVar RCV Id: RCV003341914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Thr659Ala
CA393846835
NM_001287248.2:c.1975A>G