Canonical Allele Identifier: PA2828048126
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asn509Ile
CA008624
NM_001355216.1:c.1526A>T