Canonical Allele Identifier: PA2827364782
Gene: FERRY3 HGNC NCBI

Linked Data

ClinVar Variation Id: 723335
ClinVar RCV Id: RCV000897079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333085.1:p.Ile188Thr
CA6396197
NM_001346156.2:c.563T>C