Canonical Allele Identifier: PA645485486
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Asn1348Ser
CA2393882
NM_002292.4:c.4043A>G