Canonical Allele Identifier: PA2573162613
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1478072
ClinVar RCV Id: RCV002573480 RCV003348706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Lys131Asn
CA345440202
NM_000143.4:c.393A>T
CA345440203
NM_000143.4:c.393A>C