Canonical Allele Identifier: PA257455
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 16231
ClinVar RCV Id: RCV000017618 RCV002426509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Glu362Gln
CA257453
NM_000143.4:c.1084G>C