Canonical Allele Identifier: PA2742037597
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2602907
ClinVar RCV Id: RCV003352175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Val498Met
CA10073382
NM_206965.2:c.1492G>A