Canonical Allele Identifier: PA325183
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214419
ClinVar RCV Id: RCV000200592 RCV001017278 RCV002291591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ser366Asn
CA325181
NM_000143.4:c.1097G>A