Canonical Allele Identifier: PA2826738219
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 485345
ClinVar RCV Id: RCV000575877 RCV001043175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Asn1021Asp
CA274767385
NM_001287246.2:c.3061A>G