Canonical Allele Identifier: PA2580107087
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1770453
ClinVar RCV Id: RCV002387801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Met449Leu
CA345436477
NM_000143.4:c.1345A>T
CA345436480
NM_000143.4:c.1345A>C