Canonical Allele Identifier: PA645382543
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 405934
ClinVar RCV Id: RCV000466487 RCV001018184 RCV001546164 RCV003320644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg101Gln
CA1478716
NM_000143.4:c.302G>A