Canonical Allele Identifier: PA915971389
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 639132
ClinVar RCV Id: RCV000791862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001087241.1:p.Ala493Thr
CA356906482
NM_001093772.2:c.1477G>A