Canonical Allele Identifier: PA2829018455
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_001372215.1:p.Val497Leu
CA356906532
NM_001385286.1:c.1489G>T
CA356906534
NM_001385286.1:c.1489G>C