Canonical Allele Identifier: PA2828047730
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24928
ClinVar RCV Id: RCV000121978 RCV000148770 RCV000163375 RCV000224141 RCV001104573 RCV000663272 RCV001082257 RCV001104575 RCV001533539 RCV001104572 RCV001104574
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ser395Leu
CA008470
NM_001355216.1:c.1184C>T
CA645541253
NM_001355216.1:c.1184_1185delinsTA