Canonical Allele Identifier: PA2829022684
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1710035
ClinVar RCV Id: RCV002290377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Tyr550Asp
CA356907435
NM_001385292.1:c.1648T>G