Canonical Allele Identifier: PA915960652
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 666168
ClinVar RCV Id: RCV002536030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Leu315Pro
CA345438358
NM_000143.4:c.944T>C