Canonical Allele Identifier: PA2826741547
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1055445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Tyr620Phe
CA7738903
NM_001287248.2:c.1859A>T