Canonical Allele Identifier: PA2826741559
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1000412
ClinVar RCV Id: RCV001296536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Thr624Ile
CA393846583
NM_001287248.2:c.1871C>T