Canonical Allele Identifier: PA1139690912
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 970379
ClinVar RCV Id: RCV001245944 RCV002281179 RCV002319682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Met651Val
CA7738938
NM_001287248.2:c.1951A>G