Canonical Allele Identifier: PA161939
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asp102Asn
CA009176
NM_020975.6:c.304G>A