Canonical Allele Identifier: PA319972
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 214430
ClinVar RCV Id: RCV000195609 RCV000204400 RCV000346414 RCV000568788 RCV001818470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg3Gly
CA319970
NM_000143.4:c.7C>G