Canonical Allele Identifier: PA2580196987
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 1797313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Ala964Val
CA393846359
NM_001287247.2:c.2891C>T