Canonical Allele Identifier: PA2580135081
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2372979
ClinVar RCV Id: RCV003004510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Ser137Thr
CA1375977
NM_001127641.1:c.409T>A