ClinGen Allele Registry
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Canonical Allele Identifier:
PA645383030
Gene: FH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
364940
ClinVar RCV:
RCV000430394
RCV001019060
ClinVar Variation:
392178
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000134.2:p.Ala308Gly
CA16603595
NM_000143.4:c.923C>G