Canonical Allele Identifier: PA658670317
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val240Leu
CA044589
NM_020975.6:c.718G>C
CA376544709
NM_020975.6:c.718G>T