Canonical Allele Identifier: PA2825315111
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 554258
ClinVar RCV Id: RCV000669859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Cys290Ser
CA344593678
NM_001017402.2:c.869G>C
CA344593688
NM_001017402.2:c.868T>A