Canonical Allele Identifier: PA2826168561
Gene: PDYN HGNC NCBI

Linked Data

ClinVar Variation Id: 18461
ClinVar RCV Id: RCV000018097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177827.1:p.Arg212Trp
CA257557
NM_001190898.3:c.634C>T