Canonical Allele Identifier: PA2828971169
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000425679
ClinVar Variation:
376148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Asp815Val
CA16602605
NM_001385286.1:c.2444A>T