Canonical Allele Identifier: PA915960535
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 825206
ClinVar RCV Id: RCV001023109 RCV002550882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala161Thr
CA345440008
NM_000143.4:c.481G>A