Canonical Allele Identifier: PA2829023213
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Asp816His
CA16602407
NM_001385292.1:c.2446G>C