Canonical Allele Identifier: PA2829021917
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV001226141
ClinVar Variation:
953798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Asp820Ala
CA356911952
NM_001385290.1:c.2459A>C