Canonical Allele Identifier: PA2580276706
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2301770
ClinVar RCV Id: RCV002874306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Leu1495Gln
CA352692388
NM_002292.4:c.4484T>A