Canonical Allele Identifier: PA658680471
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 460340
ClinVar RCV Id: RCV001010798 RCV001098856 RCV000543314 RCV002527719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Thr431Ile
CA40327543
NM_000143.4:c.1292C>T