Canonical Allele Identifier: PA2580196992
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 2447177
ClinVar RCV Id: RCV003165100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274176.1:p.Leu966Phe
CA7738892
NM_001287247.2:c.2896C>T