Canonical Allele Identifier: PA2829018521
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1779283
ClinVar RCV Id: RCV002401482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Trp578Leu
CA356907621
NM_001385286.1:c.1733G>T