Canonical Allele Identifier: PA658818854
Gene: EPS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 501016
ClinVar RCV Id: RCV000596501 RCV003935619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004438.3:p.Pro626Thr
CA6467417
NM_004447.6:c.1876C>A