Canonical Allele Identifier: PA2829938968
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1790712
ClinVar RCV Id: RCV002450247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ala8Val
CA376768041
NM_020630.6:c.23C>T