Canonical Allele Identifier: PA159748
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 134417
ClinVar RCV Id: RCV000121093 RCV000554866 RCV000567053 RCV002514641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met380Val
CA159746
NM_000143.4:c.1138A>G