Canonical Allele Identifier: PA175616
Gene: CTF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 163017
ClinVar RCV Id: RCV000150375 RCV000537947 RCV000765288 RCV000852714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001321.1:p.Ala92Glu
CA175614
NM_001330.5:c.275C>A