Canonical Allele Identifier: PA197799
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 187498
ClinVar RCV Id: RCV000167232 RCV000553159 RCV002485039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val351Ile
CA007417
NM_020975.6:c.1051G>A