ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826594399
Gene: ETFDH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
203715
ClinVar RCV Id:
RCV000185892
RCV001079922
RCV001199401
RCV003937656
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268667.1:p.Gly130Asp
CA312529
NM_001281738.1:c.389G>A