Canonical Allele Identifier: PA2741813134
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2717148
ClinVar RCV Id: RCV003548646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Pro304Ala
CA345438426
NM_000143.4:c.910C>G