Canonical Allele Identifier: PA915969435
Gene: HHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 771435
ClinVar RCV Id: RCV000950750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002720.1:p.Ser234Cys
CA5604725
NM_002729.5:c.701C>G