Canonical Allele Identifier: PA337724
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216722
ClinVar RCV Id: RCV000198200 RCV000662775 RCV000679738 RCV001017530 RCV003462337 RCV002492921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser977Arg
CA041466
NM_020630.6:c.2931C>G
CA376557985
NM_020630.6:c.2929A>C
CA376557989
NM_020630.6:c.2931C>A