Canonical Allele Identifier: PA891847824
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 569870
ClinVar RCV Id: RCV001014923 RCV001662755 RCV003153803 RCV000690605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr75Met
CA038004
NM_020975.6:c.224C>T