Canonical Allele Identifier: PA658680218
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 485563
ClinVar RCV Id: RCV000574732 RCV002491134 RCV002530335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp65Val
CA40335952
NM_000143.4:c.194A>T