ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573162626
Gene: FH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1379338
ClinVar RCV Id:
RCV002552286
RCV003303277
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000134.2:p.Ala161Val
CA345440003
NM_000143.4:c.482C>T