Canonical Allele Identifier: PA2573317040
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1627789
ClinVar RCV Id: RCV002133000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Gly336Val
CA10073624
NM_206965.2:c.1007G>T