Canonical Allele Identifier: PA658818851
Gene: EPS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 500289
ClinVar RCV Id: RCV000592406
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004438.3:p.Lys608Gln
CA6467431
NM_004447.6:c.1822A>C