Canonical Allele Identifier: PA2826741529
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 405273
ClinVar RCV Id: RCV000456674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Ile611Thr
CA16614962
NM_001287248.2:c.1832T>C