Canonical Allele Identifier: PA2825474894
Gene: P2RY14 HGNC NCBI
ClinVar RCV:
RCV000903939
ClinVar Variation:
729312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001074924.1:p.Pro301Leu
CA2667074
NM_001081455.2:c.902C>T