Canonical Allele Identifier: PA915967616
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295132
ClinVar RCV Id: RCV000319455 RCV002522100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Leu224Pro
CA1375875
NM_001127641.1:c.671T>C