Canonical Allele Identifier: PA2829019558
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1004231
ClinVar RCV Id: RCV001300905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Pro468Ser
CA356906315
NM_001385288.1:c.1402C>T