Canonical Allele Identifier: PA2826740224
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 133705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Ser1237Pro
CA157406
NM_001287247.2:c.3709T>C