Canonical Allele Identifier: PA2826738916
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 824545
ClinVar RCV Id: RCV001021764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Ser1352Phe
CA393851505
NM_001287246.2:c.4055C>T