Canonical Allele Identifier: PA2828971186
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375931
ClinVar Variation Id: 375932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Asn817Lys
CA16602411
NM_001385286.1:c.2451T>A
CA16602412
NM_001385286.1:c.2451T>G