Canonical Allele Identifier: PA2828048467
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24947
ClinVar RCV Id: RCV000148778 RCV000575365 RCV000662511 RCV000691895 RCV000782197 RCV001818175 RCV001535741 RCV002477003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Pro587Leu
CA008837
NM_001355216.1:c.1760C>T