Canonical Allele Identifier: PA2825316190
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2263909
ClinVar RCV Id: RCV002798264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Arg1009Leu
CA36749836
NM_001017402.2:c.3026G>T