Canonical Allele Identifier: PA2829021922
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375931
ClinVar RCV Id: RCV000429954 RCV000419670 RCV000436687 RCV001269701
ClinVar Variation Id: 375932
ClinVar RCV Id: RCV000419001 RCV000429190 RCV000439434 RCV001269906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Asn822Lys
CA16602411
NM_001385290.1:c.2466T>A
CA16602412
NM_001385290.1:c.2466T>G