Canonical Allele Identifier: PA2829022694
Gene: KIT HGNC NCBI
ClinVar RCV:
RCV000439662
ClinVar Variation:
376734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Trp554Cys
CA16603142
NM_001385292.1:c.1662G>C
CA356907466
NM_001385292.1:c.1662G>T