Canonical Allele Identifier: PA891847854
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 568416
ClinVar RCV Id: RCV000688770 RCV001103793 RCV001103794 RCV001103791 RCV001103792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro162Ser
CA376543214
NM_020975.6:c.484C>T