Canonical Allele Identifier: PA915967705
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 295103
ClinVar RCV Id: RCV000392698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121113.1:p.Arg539Trp
CA1375515
NM_001127641.1:c.1615C>T