Canonical Allele Identifier: PA2741812895
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2567080
ClinVar RCV Id: RCV003278320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Gly69Ser
CA345441832
NM_000143.4:c.205G>A