Canonical Allele Identifier: PA2825474894
Gene: P2RY14 HGNC NCBI

Linked Data

ClinVar Variation Id: 729312
ClinVar RCV Id: RCV000903939

Amino-acid Alleles

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