Canonical Allele Identifier: PA2580106975
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2003649
ClinVar RCV Id: RCV002811338
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr234Ser
CA345439214
NM_000143.4:c.701C>G
CA345439216
NM_000143.4:c.700A>T