Canonical Allele Identifier: PA2828970279
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Gly561Val
CA215587
NM_001385286.1:c.1682G>T