Canonical Allele Identifier: PA2828963204
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372213.1:p.Trp558Gly
CA16603140
NM_001385284.1:c.1672T>G