Canonical Allele Identifier: PA285321
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 92447
ClinVar RCV Id: RCV000078140 RCV000220396 RCV000445596 RCV003460741 RCV004555535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Asn340Lys
CA285319
NM_000143.4:c.1020T>A
CA345438206
NM_000143.4:c.1020T>G