Canonical Allele Identifier: PA174590
Gene: ULK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161681
ClinVar RCV Id: RCV000149217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055498.3:p.Ala172Ser
CA174589
NM_014683.4:c.514G>T