Canonical Allele Identifier: PA2825315272
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2501055
ClinVar RCV Id: RCV003226652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Arg366Trp
CA1375702
NM_001017402.2:c.1096C>T