Canonical Allele Identifier: PA2830524648
Gene: FTCD HGNC NCBI
ClinVar RCV:
RCV003816182
ClinVar Variation:
2954983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Ala525Val
CA410555622
NM_206965.2:c.1574C>T