Canonical Allele Identifier: PA2826738141
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 454123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274175.1:p.Ser987Phe
CA393846503
NM_001287246.2:c.2960C>T