Canonical Allele Identifier: PA2829941939
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1789038
ClinVar RCV Id: RCV002446186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Asn763Ser
CA376555531
NM_020630.6:c.2288A>G