Canonical Allele Identifier: PA645488039
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 237252
ClinVar RCV Id: RCV000234428 RCV000282556 RCV000332028 RCV000503289 RCV000764541 RCV001535624 RCV001014023 RCV001753684 RCV003919917
ClinVar Variation Id: 2159404
ClinVar RCV Id: RCV003093773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Thr67Ser
CA2923186
NM_000222.3:c.199A>T
CA2923187
NM_000222.3:c.200C>G