Canonical Allele Identifier: PA106845
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13911
ClinVar RCV Id: RCV000014930 RCV000014928 RCV000014929 RCV000471652 RCV002408463 RCV003237413
ClinVar Variation Id: 2025097
ClinVar RCV Id: RCV002848185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys634Phe
CA008370
NM_020975.6:c.1901G>T
CA2580081463
NM_020975.6:c.1901_1902delinsTT