Canonical Allele Identifier: PA2825315019
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Arg230Thr
CA1375872
NM_001017402.2:c.689G>C