Canonical Allele Identifier: PA106833
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13908
ClinVar RCV Id: RCV000014923 RCV000014922 RCV000182581 RCV001310209 RCV001420921 RCV000654584 RCV001013616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys634Gly
CA008324
NM_020975.6:c.1900T>G