Canonical Allele Identifier: PA2580106911
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1995034
ClinVar RCV Id: RCV002791580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Arg160Ser
CA345440009
NM_000143.4:c.480A>T
CA345440010
NM_000143.4:c.480A>C