Canonical Allele Identifier: PA2829019562
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 528497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Phe470Leu
CA356906323
NM_001385288.1:c.1408T>C
CA356906328
NM_001385288.1:c.1410T>A
CA356906329
NM_001385288.1:c.1410T>G