Canonical Allele Identifier: PA2828966553
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Gly664Arg
CA123500
NM_001385285.1:c.1990G>A
CA356908804
NM_001385285.1:c.1990G>C