Canonical Allele Identifier: PA2826741532
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 454123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Ser612Phe
CA393846503
NM_001287248.2:c.1835C>T