Canonical Allele Identifier: PA915967708
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 763952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg539Gln
CA1375514
NM_001127641.1:c.1616G>A