Canonical Allele Identifier: PA112490
Gene: LAMB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 14552
ClinVar RCV Id: RCV000015653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000219.2:p.Lys207Gln
CA257287
NM_000228.3:c.619A>C