Canonical Allele Identifier: PA1139690384
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 843255
ClinVar RCV Id: RCV001045833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Tyr974Ser
CA393846420
NM_001287247.2:c.2921A>C