Canonical Allele Identifier: PA2828048737
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13919
ClinVar RCV Id: RCV000014941 RCV000014942 RCV000014943 RCV000082054 RCV000175096 RCV000161926 RCV000417859 RCV000415312 RCV000425499 RCV000428538 RCV000444529 RCV000999916 RCV001292662 RCV001542764 RCV002255998 RCV004532351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Met664Thr
CA009082
NM_001355216.1:c.1991T>C