Canonical Allele Identifier: PA2826146119
Gene: PARD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 720817
ClinVar RCV Id: RCV000894197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171716.1:p.Ser801Asn
CA5467637
NM_001184787.2:c.2402G>A