Canonical Allele Identifier: PA2573191941
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1410176
ClinVar RCV Id: RCV001916319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Leu629His
CA393846612
NM_001287248.2:c.1886T>A