Canonical Allele Identifier: PA103999
Gene: LAMB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 14530
ClinVar RCV Id: RCV000015629 RCV001335017 RCV001849266 RCV002504793
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002283.3:p.Arg246Trp
CA124107
NM_002292.4:c.736C>T