Canonical Allele Identifier: PA2826738096
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1797313
ClinVar RCV Id: RCV002437938 RCV003102842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Ala964Val
CA393846359
NM_001287246.2:c.2891C>T