Canonical Allele Identifier: PA2825315842
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_001017402.1:p.Gly761del
CA1375293
NM_001017402.2:c.2280_2282del
CA344588360
NM_001017402.2:c.2278G>T
CA344588366
NM_001017402.2:c.2275G>T
CA344588373
NM_001017402.2:c.2272G>T