Canonical Allele Identifier: PA325229
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214377
ClinVar RCV Id: RCV000200636 RCV000467363 RCV000572182 RCV003387797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala273Thr
CA325227
NM_000143.4:c.817G>A