Canonical Allele Identifier: PA2829021920
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000425679
ClinVar Variation:
376148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Asp820Val
CA16602605
NM_001385290.1:c.2459A>T