Canonical Allele Identifier: PA2826984921
Gene: FHOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 156714
ClinVar RCV Id: RCV000190292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305131.1:p.Ala212Val
CA248418
NM_001318202.2:c.635C>T