ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA915960559
Gene: FH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
825940
ClinVar RCV Id:
RCV001024482
RCV001100768
RCV001098959
RCV002551893
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000134.2:p.Pro192Ser
CA345439470
NM_000143.4:c.574C>T