Canonical Allele Identifier: PA658803241
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 528497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Phe469Leu
CA356906323
NM_000222.3:c.1405T>C
CA356906328
NM_000222.3:c.1407T>A
CA356906329
NM_000222.3:c.1407T>G