Canonical Allele Identifier: PA2828970544
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1716574
ClinVar RCV Id: RCV002295893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Met634Leu
CA356908521
NM_001385286.1:c.1900A>T
CA356908523
NM_001385286.1:c.1900A>C