ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826594859
Gene: ETFDH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
361463
ClinVar RCV:
RCV000415983
RCV000763116
ClinVar Variation:
374577
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268667.1:p.Pro395Ser
CA3122610
NM_001281738.1:c.1183C>T