Canonical Allele Identifier: PA2825315528
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295102
ClinVar RCV Id: RCV000335162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Arg556Cys
CA1375500
NM_001017402.2:c.1666C>T