Canonical Allele Identifier: PA106269
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12302
ClinVar RCV Id: RCV000013096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002520.2:p.Gly577Arg
CA256262
NM_002529.4:c.1729G>C