Canonical Allele Identifier: PA2573223301
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505990
ClinVar RCV Id: RCV001999657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Ala1347Thr
CA352697173
NM_002292.4:c.4039G>A