Canonical Allele Identifier: PA2828970558
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 376440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Lys638Asn
CA16602875
NM_001385286.1:c.1914A>C
CA356908602
NM_001385286.1:c.1914A>T