Allele Registry

Canonical Allele Identifier: PA1139670120

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV001228656

ClinVar Variation:

955935

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Val559Phe	CA356907472 NM_000222.3:c.1675G>T