Canonical Allele Identifier: PA891846608
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 571575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Pro518Ser
CA356906890
NM_000222.3:c.1552C>T