Canonical Allele Identifier: PA2826168471
Gene: PDYN HGNC NCBI

Linked Data

ClinVar Variation Id: 447927
ClinVar RCV Id: RCV000517756 RCV000900279 RCV002490885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177827.1:p.Gly36Cys
CA9730383
NM_001190898.3:c.106G>T