Canonical Allele Identifier: PA658818856
Gene: EPS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 508572
ClinVar RCV Id: RCV000953310 RCV000606854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004438.3:p.Ala705Thr
CA6467353
NM_004447.6:c.2113G>A