Canonical Allele Identifier: PA645488368
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Met651Leu
CA2923614
NM_000222.3:c.1951A>T
CA356908723
NM_000222.3:c.1951A>C