Canonical Allele Identifier: PA2828047681
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241341
ClinVar RCV Id: RCV000226795 RCV000410332 RCV000409197 RCV000679725 RCV001013684 RCV003469160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ala385Thr
CA036557
NM_001355216.1:c.1153G>A