Canonical Allele Identifier: PA2826738908
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2759672
ClinVar RCV Id: RCV003504960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Gln1343Glu
CA393851336
NM_001287246.2:c.4027C>G