Canonical Allele Identifier: PA916043112
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13948
ClinVar RCV Id: RCV000014975 RCV000410425 RCV000148783 RCV000411688 RCV000563865 RCV000704911 RCV002490367 RCV003398513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Pro785Leu
CA009200
NM_001355216.1:c.2354C>T