Canonical Allele Identifier: PA915967892
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295060
ClinVar RCV Id: RCV000321360 RCV000957522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.His1160Arg
CA1374844
NM_001127641.1:c.3479A>G