Canonical Allele Identifier: PA2828970020
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 847706
ClinVar RCV Id: RCV001051304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Phe483Leu
CA356906414
NM_001385286.1:c.1447T>C
CA356906419
NM_001385286.1:c.1449C>A
CA356906420
NM_001385286.1:c.1449C>G