Canonical Allele Identifier: PA2829019592
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 847706
ClinVar RCV Id: RCV001051304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Phe484Leu
CA356906414
NM_001385288.1:c.1450T>C
CA356906419
NM_001385288.1:c.1452C>A
CA356906420
NM_001385288.1:c.1452C>G