Canonical Allele Identifier: PA2829946938
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2048904
ClinVar RCV Id: RCV002909429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asn113Asp
CA376770602
NM_020975.6:c.337A>G