Canonical Allele Identifier: PA658827050
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 546624
ClinVar RCV Id: RCV000658544 RCV003163032
ClinVar Variation Id: 591326
ClinVar RCV Id: RCV000722504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Ala1145Val
CA1374859
NM_000228.3:c.3434C>T
CA891862877
NM_000228.3:c.3432_3434delinsGGT