Canonical Allele Identifier: PA257452
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 16230
ClinVar RCV Id: RCV000017617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala265Thr
CA257450
NM_000143.4:c.793G>A