Canonical Allele Identifier: PA2825316091
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2349916
ClinVar RCV Id: RCV002956843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Met932Thr
CA1375094
NM_001017402.2:c.2795T>C