Canonical Allele Identifier: PA2828970577
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Met647Leu
CA2923614
NM_001385286.1:c.1939A>T
CA356908723
NM_001385286.1:c.1939A>C