Canonical Allele Identifier: PA658668304
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477369
ClinVar RCV Id: RCV000535690 RCV001294031 RCV001811073 RCV002448801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro1067Leu
CA054768
NM_020975.6:c.3200C>T