Canonical Allele Identifier: PA2829946914
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3065760
ClinVar RCV Id: RCV003990837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly93Ser
CA376770471
NM_020975.6:c.277G>A