Canonical Allele Identifier: PA2826293027
Gene: FCER2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2361041
ClinVar RCV Id: RCV004198967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193948.2:p.Ser218Phe
CA9144959
NM_001207019.2:c.653C>T