Allele Registry

Canonical Allele Identifier: PA2828970066

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000430398

ClinVar Variation:

375904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Phe504Leu	CA16602387 NM_001385286.1:c.1510T>C CA356906628 NM_001385286.1:c.1512T>A CA356906630 NM_001385286.1:c.1512T>G