Canonical Allele Identifier: PA2828966093
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Trp557Gly
CA16603140
NM_001385285.1:c.1669T>G