Canonical Allele Identifier: PA215568
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 41585
ClinVar RCV Id: RCV000034487 RCV000332300 RCV000381370 RCV001011508 RCV004555533
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr474Arg
CA215566
NM_000143.4:c.1421C>G