Canonical Allele Identifier: PA2828970543
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1037658
ClinVar RCV Id: RCV001340847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Met634Ile
CA356908534
NM_001385286.1:c.1902G>A
CA356908536
NM_001385286.1:c.1902G>C
CA356908538
NM_001385286.1:c.1902G>T