Canonical Allele Identifier: PA645478246
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_006648.1:p.Val99Ala
CA10073978
NM_006657.3:c.296T>C