Canonical Allele Identifier: PA2825063652
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1709012
ClinVar RCV Id: RCV002288296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu353_Gly364dup
CA2580063485
NM_000143.4:c.1056_1091dup