Canonical Allele Identifier: PA2826738894
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 584897
ClinVar RCV Id: RCV000709371 RCV002352229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Met1339Thr
CA7739173
NM_001287246.2:c.4016T>C