Canonical Allele Identifier: PA891846607
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 567141
ClinVar RCV Id: RCV000687137
ClinVar Variation Id: 576649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Val497Leu
CA356906532
NM_000222.3:c.1489G>T
CA356906534
NM_000222.3:c.1489G>C