Canonical Allele Identifier: PA915967669
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Glu351Lys
CA1375710
NM_001127641.1:c.1051G>A