Canonical Allele Identifier: PA658680232
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460353
ClinVar RCV Id: RCV000530788 RCV000765097 RCV002528327 RCV002358479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala128Thr
CA345440227
NM_000143.4:c.382G>A