Canonical Allele Identifier: PA2573162633
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1372774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ser171Arg
CA345439934
NM_000143.4:c.513C>G
CA345439935
NM_000143.4:c.513C>A
CA345439939
NM_000143.4:c.511A>C