Canonical Allele Identifier: PA2825315705
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 552193
ClinVar RCV Id: RCV000667415 RCV002307584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Pro679Leu
CA1375398
NM_001017402.2:c.2036C>T