Canonical Allele Identifier: PA106764
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13943
ClinVar Variation Id: 38602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys620Ser
CA008047
NM_020975.6:c.1858T>A
CA008085
NM_020975.6:c.1859G>C