Canonical Allele Identifier: PA2829949047
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227534
ClinVar RCV Id: RCV004524652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gln860His
CA376556711
NM_020975.6:c.2580G>C
CA376556716
NM_020975.6:c.2580G>T