Canonical Allele Identifier: PA2829019717
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_001372217.1:p.Met549Ile
CA356907431
NM_001385288.1:c.1647G>A
CA356907432
NM_001385288.1:c.1647G>T
CA356907433
NM_001385288.1:c.1647G>C