Canonical Allele Identifier: PA2580440934
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1771753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr5Ala
CA376768019
NM_020975.6:c.13A>G