Canonical Allele Identifier: PA2580243092
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 2076028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Ser477Thr
CA356906370
NM_001385292.1:c.1430G>C