Canonical Allele Identifier: PA645485490
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 345977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Lys1497Glu
CA2393776
NM_002292.4:c.4489A>G