Canonical Allele Identifier: PA645488250
Gene: KIT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Val560Glu
CA16603143
NM_000222.3:c.1679_1680delinsAA
CA645516868
NM_000222.3:c.1679_1680delinsAG