Canonical Allele Identifier: PA2825316311
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 546624
ClinVar Variation Id: 591326
ClinVar RCV Id: RCV000722504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017402.1:p.Ala1145Val
CA1374859
NM_001017402.2:c.3434C>T
CA891862877
NM_001017402.2:c.3432_3434delinsGGT