Canonical Allele Identifier: PA658670268
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser100Asn
CA376770519
NM_020975.6:c.299G>A