Canonical Allele Identifier: PA204099
Gene: SYK HGNC NCBI

Linked Data

ClinVar Variation Id: 207858
ClinVar RCV Id: RCV000190148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128524.1:p.Ala52Ser
CA204098
NM_001135052.4:c.154G>T