Canonical Allele Identifier: PA916043067
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477393
ClinVar RCV Id: RCV000528670 RCV000566312 RCV000709105 RCV003459267 RCV003327423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ala71Thr
CA045679
NM_001355216.1:c.211G>A