Canonical Allele Identifier: PA257558
Gene: PDYN HGNC NCBI
ClinVar RCV:
RCV000018097
ClinVar Variation:
18461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077722.1:p.Arg212Trp
CA257557
NM_024411.5:c.634C>T