Canonical Allele Identifier: PA2826740994
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 646436
ClinVar RCV Id: RCV000800717 RCV003344057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Thr363Ala
CA393844800
NM_001287248.2:c.1087A>G