Canonical Allele Identifier: PA2825315276
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2267517
ClinVar RCV Id: RCV002804160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Pro368Leu
CA1375698
NM_001017402.2:c.1103C>T