Canonical Allele Identifier: PA128309
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24928
ClinVar RCV Id: RCV000121978 RCV000148770 RCV000163375 RCV000224141 RCV001104573 RCV000663272 RCV001082257 RCV001104575 RCV001533539 RCV001104572 RCV001104574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser649Leu
CA008470
NM_020630.6:c.1946C>T
CA645541253
NM_020630.6:c.1946_1947delinsTA