Canonical Allele Identifier: PA2828970007
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 528520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Ser481Arg
CA356906401
NM_001385286.1:c.1441A>C
CA356906406
NM_001385286.1:c.1443T>A
CA356906407
NM_001385286.1:c.1443T>G