Canonical Allele Identifier: PA658680166
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460359
ClinVar RCV Id: RCV001023401 RCV003459206 RCV004555584 RCV001662540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Tyr2His
CA1478785
NM_000143.4:c.4T>C