Canonical Allele Identifier: PA2829020216
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1445071
ClinVar RCV Id: RCV001982730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Asn794Ser
CA356911513
NM_001385288.1:c.2381A>G