Canonical Allele Identifier: PA110215
Gene: PDYN HGNC NCBI

Linked Data

ClinVar Variation Id: 18459
ClinVar RCV Id: RCV000018095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177821.1:p.Arg215Cys
CA257553
NM_001190892.1:c.643C>T