Canonical Allele Identifier: PA1139690903
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 966071
ClinVar RCV Id: RCV001240659 RCV002436949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Glu633Val
CA393846656
NM_001287248.2:c.1898A>T