Canonical Allele Identifier: PA2826295743
Gene: FCER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2243089
ClinVar RCV Id: RCV004105744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001207429.1:p.Cys174Ser
CA403109217
NM_001220500.2:c.521G>C
CA403109242
NM_001220500.2:c.520T>A