Canonical Allele Identifier: PA112478
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14550
ClinVar RCV Id: RCV000015651 RCV000675069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Gly199Ala
CA257285
NM_000228.3:c.596G>C