Canonical Allele Identifier: PA2826739795
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1727522
ClinVar RCV Id: RCV002325862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Ile1033Val
CA393846829
NM_001287247.2:c.3097A>G