Canonical Allele Identifier: PA104014
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Asn1380Lys
CA074242
NM_002292.4:c.4140C>A
CA352695956
NM_002292.4:c.4140C>G