Allele Registry

Canonical Allele Identifier: PA2829021587

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000430398

ClinVar Variation:

375904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Phe505Leu	CA16602387 NM_001385290.1:c.1513T>C CA356906628 NM_001385290.1:c.1515T>A CA356906630 NM_001385290.1:c.1515T>G