Canonical Allele Identifier: PA248419
Gene: FHOD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 156714
ClinVar RCV Id: RCV000190292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037373.2:p.Ala212Val
CA248418
NM_013241.2:c.635C>T