Canonical Allele Identifier: PA2826168744
Gene: PDYN HGNC NCBI

Linked Data

ClinVar Variation Id: 18461
ClinVar RCV Id: RCV000018097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177828.1:p.Arg212Trp
CA257557
NM_001190899.2:c.634C>T