Canonical Allele Identifier: PA645383042
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 237119
ClinVar RCV Id: RCV000230405 RCV001589168 RCV002372248 RCV002487046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro309Leu
CA1478570
NM_000143.4:c.926C>T