Canonical Allele Identifier: PA2828963239
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372213.1:p.Gly566Val
CA215587
NM_001385284.1:c.1697G>T