Canonical Allele Identifier: PA645487965
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 405273
ClinVar RCV Id: RCV000456674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000048.1:p.Ile986Thr
CA16614962
NM_000057.4:c.2957T>C