Canonical Allele Identifier: PA2742019986
Gene: P2RY13 HGNC NCBI
ClinVar RCV:
RCV004308426
ClinVar Variation:
2533867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_795713.2:p.Ile165Thr
CA354976071
NM_176894.3:c.494T>C