Canonical Allele Identifier: PA325332
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214422
ClinVar RCV Id: RCV000200752 RCV000445595 RCV000465210 RCV002336534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly397Arg
CA325330
NM_000143.4:c.1189G>A
CA345437388
NM_000143.4:c.1189G>C