Canonical Allele Identifier: PA645382507
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 296875
ClinVar RCV Id: RCV000338926 RCV000387476 RCV000570874 RCV002520481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn64Asp
CA10609927
NM_000143.4:c.190A>G