Canonical Allele Identifier: PA192363
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 185591
ClinVar RCV Id: RCV000165037 RCV000349307 RCV000388495 RCV001582651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000134.2:p.Ala102Val
CA192361
NM_000143.4:c.305C>T