Canonical Allele Identifier: PA2829023219
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375931
ClinVar Variation Id: 375932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Asn818Lys
CA16602411
NM_001385292.1:c.2454T>A
CA16602412
NM_001385292.1:c.2454T>G