Canonical Allele Identifier: PA2825095293
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2349916
ClinVar RCV Id: RCV002956843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Met932Thr
CA1375094
NM_000228.3:c.2795T>C