Canonical Allele Identifier: PA916071307
Gene: PARD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 720817
ClinVar RCV Id: RCV000894197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062565.2:p.Ser801Asn
CA5467637
NM_019619.4:c.2402G>A