Canonical Allele Identifier: PA287051
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 127472
ClinVar RCV Id: RCV000115278 RCV000477302 RCV000574582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000048.1:p.Ile366Thr
CA287049
NM_000057.4:c.1097T>C