Canonical Allele Identifier: PA356786
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 219791
ClinVar RCV Id: RCV000205293 RCV002399761 RCV003153481 RCV003462370
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val351Glu
CA030932
NM_020975.6:c.1052T>A