Canonical Allele Identifier: PA2829018483
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Trp553Phe
CA16603144
NM_001385286.1:c.1658_1659delinsTT