Canonical Allele Identifier: PA2580441021
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1790999
ClinVar RCV Id: RCV002459781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.His81Tyr
CA376770382
NM_020975.6:c.241C>T