Canonical Allele Identifier: PA120117
Gene: NTRK2 HGNC NCBI
ClinVar RCV:
RCV000009698
ClinVar Variation:
9127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006171.2:p.Tyr722Cys
CA120116
NM_006180.6:c.2165A>G