Canonical Allele Identifier: PA159751
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 134418
ClinVar RCV Id: RCV000121094 RCV000473170 RCV001564388 RCV000571469 RCV004555537 RCV003325184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Val435Met
CA159749
NM_000143.4:c.1303G>A