Canonical Allele Identifier: PA916043122
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241358
ClinVar RCV Id: RCV000225774 RCV000563947 RCV000679746 RCV001196701 RCV003463679 RCV003492013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Arg796Gln
CA042811
NM_001355216.1:c.2387G>A