Canonical Allele Identifier: PA891845686
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 584503
ClinVar RCV Id: RCV000708667 RCV000810866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000048.1:p.Ile1005Thr
CA7738908
NM_000057.4:c.3014T>C