Canonical Allele Identifier: PA102947
Gene: SPRY4 HGNC NCBI

Linked Data

ClinVar Variation Id: 50874
ClinVar RCV Id: RCV000043616 RCV000454560 RCV001849295 RCV000954651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120968.1:p.Ser218Tyr
CA143835
NM_001127496.3:c.653C>A