Canonical Allele Identifier: PA2825316185
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2206873
ClinVar RCV Id: RCV002641551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Arg1006His
CA1375016
NM_001017402.2:c.3017G>A