Canonical Allele Identifier: PA2829018546
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000421498
ClinVar Variation:
376058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Thr666Ile
CA16602525
NM_001385286.1:c.1997C>T