Canonical Allele Identifier: PA2826168886
Gene: PDYN HGNC NCBI
ClinVar RCV:
RCV000018097
ClinVar Variation:
18461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177829.1:p.Arg212Trp
CA257557
NM_001190900.1:c.634C>T