Canonical Allele Identifier: PA2829021916
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000427793
ClinVar Variation:
375927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Asp820His
CA16602407
NM_001385290.1:c.2458G>C