Canonical Allele Identifier: PA2825092018
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1004231
ClinVar RCV Id: RCV001300905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Pro467Ser
CA356906315
NM_000222.3:c.1399C>T