Canonical Allele Identifier: PA916035685
Gene: FERRY3 HGNC NCBI
ClinVar RCV:
RCV000897079
ClinVar Variation:
723335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339891.1:p.Ile77Thr
CA6396197
NM_001352962.2:c.230T>C