Canonical Allele Identifier: PA658680166
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr2His
CA1478785
NM_000143.4:c.4T>C