Canonical Allele Identifier: PA2573077957
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000417409
ClinVar Variation:
376732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Trp558Gly
CA16603140
NM_001385290.1:c.1672T>G