Canonical Allele Identifier: PA1139678594
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 937464
ClinVar RCV Id: RCV002561226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ile157Val
CA1478677
NM_000143.4:c.469A>G