Canonical Allele Identifier: PA2826112867
Gene: SYK HGNC NCBI

Linked Data

ClinVar Variation Id: 207858
ClinVar RCV Id: RCV000190148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167639.1:p.Ala52Ser
CA204098
NM_001174168.3:c.154G>T