Canonical Allele Identifier: PA916073789
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 393153
ClinVar RCV Id: RCV000436784 RCV001089091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Val99Ala
CA10073978
NM_206965.2:c.296T>C