Canonical Allele Identifier: PA915967718
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295100
ClinVar RCV Id: RCV000379413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Pro557Leu
CA1375497
NM_001127641.1:c.1670C>T