Canonical Allele Identifier: PA2829647174
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2602907
ClinVar RCV Id: RCV003352175
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Val498Met
CA10073382
NM_006657.3:c.1492G>A