Canonical Allele Identifier: PA189213
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 42094
ClinVar RCV Id: RCV000034920 RCV000163798 RCV000199873 RCV001762109 RCV002280864
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gln376Pro
CA189211
NM_000143.4:c.1127A>C