Canonical Allele Identifier: PA2825094796
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2267517
ClinVar RCV Id: RCV002804160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Pro368Leu
CA1375698
NM_000228.3:c.1103C>T