Canonical Allele Identifier: PA2825315123
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803490
ClinVar RCV Id: RCV002467160 RCV003403841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Cys293Ser
CA1375797
NM_001017402.2:c.877T>A
CA344593626
NM_001017402.2:c.878G>C