Canonical Allele Identifier: PA1139679271
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 864859
ClinVar RCV Id: RCV003128750 RCV001072142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn390Ser
CA345437446
NM_000143.4:c.1169A>G