Canonical Allele Identifier: PA203920
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 203994
ClinVar RCV Id: RCV000186216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Ser45Ala
CA203919
NM_000228.3:c.133T>G