Canonical Allele Identifier: PA2829019820
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13864
ClinVar RCV Id: RCV000014878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Phe581Cys
CA123543
NM_001385288.1:c.1742T>G