Canonical Allele Identifier: PA2829021202
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Thr305Ala
CA215605
NM_001385290.1:c.913A>G