Canonical Allele Identifier: PA2829020252
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Asp817His
CA16602407
NM_001385288.1:c.2449G>C