Canonical Allele Identifier: PA915960455
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 818892
ClinVar RCV Id: RCV001010940 RCV002549331
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala45Ser
CA345442071
NM_000143.4:c.133G>T