Canonical Allele Identifier: PA2826738106
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1797380
ClinVar RCV Id: RCV002438005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Pro967Ser
CA393846372
NM_001287246.2:c.2899C>T