Canonical Allele Identifier: PA233954
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 167040
ClinVar RCV Id: RCV000153200 RCV000392257 RCV001831952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004444.2:p.Pro27Ser
CA233953
NM_004453.4:c.79C>T