Canonical Allele Identifier: PA2580106914
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2452785
ClinVar RCV Id: RCV003177559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala161Glu
CA345440005
NM_000143.4:c.482C>A