Canonical Allele Identifier: PA2826293024
Gene: FCER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2243089
ClinVar RCV Id: RCV004105744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193948.2:p.Cys173Ser
CA403109217
NM_001207019.2:c.518G>C
CA403109242
NM_001207019.2:c.517T>A