Canonical Allele Identifier: PA916016406
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 405280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274177.1:p.Gly636Arg
CA7738927
NM_001287248.2:c.1906G>A
CA393846675
NM_001287248.2:c.1906G>C