Canonical Allele Identifier: PA658680287
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460370
ClinVar RCV Id: RCV000531582 RCV002527734 RCV003302803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asp216Val
CA345439320
NM_000143.4:c.647A>T