Canonical Allele Identifier: PA645488215
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000417409
ClinVar Variation:
376732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Trp557Gly
CA16603140
NM_000222.3:c.1669T>G