Canonical Allele Identifier: PA1139678974
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 591117
ClinVar RCV Id: RCV000722293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Gly761del