Canonical Allele Identifier: PA167293
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 142062
ClinVar RCV Id: RCV000130874 RCV000200494 RCV000462728 RCV003153423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala70Thr
CA167291
NM_000143.4:c.208G>A