Canonical Allele Identifier: PA2829647170
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1957014
ClinVar RCV Id: RCV002705981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Met489Leu
CA410557586
NM_006657.3:c.1465A>T
CA410557588
NM_006657.3:c.1465A>C