Canonical Allele Identifier: PA645383030
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 392178
ClinVar RCV Id: RCV000430394 RCV001019060
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala308Gly
CA16603595
NM_000143.4:c.923C>G