Canonical Allele Identifier: PA2825315446
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499257
ClinVar RCV Id: RCV003221558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Gly508Ser
CA1375555
NM_001017402.2:c.1522G>A