Canonical Allele Identifier: PA645488225
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Trp557Phe
CA16603144
NM_000222.3:c.1670_1671delinsTT