Canonical Allele Identifier: PA2829939412
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 822958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser104Arg
CA376770541
NM_020630.6:c.310A>C
CA376770547
NM_020630.6:c.312C>G
CA376770548
NM_020630.6:c.312C>A