Canonical Allele Identifier: PA1139679032
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 876950
ClinVar RCV Id: RCV001102274 RCV002554991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg1009Trp
CA1375013
NM_001127641.1:c.3025C>T