Canonical Allele Identifier: PA2826145911
Gene: PARD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 720817
ClinVar RCV Id: RCV000894197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171714.1:p.Ser798Asn
CA5467637
NM_001184785.2:c.2393G>A