Canonical Allele Identifier: PA2573077950
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 834276
ClinVar RCV Id: RCV001034924
ClinVar Variation Id: 939321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Met553Ile
CA356907431
NM_001385290.1:c.1659G>A
CA356907432
NM_001385290.1:c.1659G>T
CA356907433
NM_001385290.1:c.1659G>C