Canonical Allele Identifier: PA2829020268
Gene: KIT HGNC NCBI
ClinVar Allele:
363135
ClinVar RCV:
RCV000440432
ClinVar Variation:
376256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Val822Ala
CA16602706
NM_001385288.1:c.2465T>C