Canonical Allele Identifier: PA2825062931
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 3230436
ClinVar RCV Id: RCV004520587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala45Gly
CA345442065
NM_000143.4:c.134C>G