Canonical Allele Identifier: PA106458
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 161358
ClinVar RCV Id: RCV000148781 RCV000411751 RCV000409290 RCV000462012 RCV000455880 RCV000562835 RCV001102744 RCV001102743 RCV000766923 RCV001102745 RCV001102746 RCV004532668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg694Gln
CA008578
NM_020975.6:c.2081G>A