Canonical Allele Identifier: PA2573078011
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000014855
ClinVar Variation:
13843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Gly665Arg
CA123500
NM_001385290.1:c.1993G>A
CA356908804
NM_001385290.1:c.1993G>C