Canonical Allele Identifier: PA2573061557
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1326115
ClinVar RCV Id: RCV001786176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro63Thr
CA345441890
NM_000143.4:c.187C>A