Canonical Allele Identifier: PA915967633
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 747357
ClinVar RCV Id: RCV000924056 RCV003923306 RCV004029494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg292Leu
CA1375798
NM_001127641.1:c.875G>T