Canonical Allele Identifier: PA1139678272
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 958272
ClinVar RCV Id: RCV002563200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp55Gly
CA345441969
NM_000143.4:c.164A>G