Canonical Allele Identifier: PA1139678302
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 970010
ClinVar RCV Id: RCV002418844 RCV002568623
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr67Asp
CA345441855
NM_000143.4:c.199T>G