Canonical Allele Identifier: PA658805342
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 543749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu19del
CA043719
NM_020975.6:c.56_58del
CA2608894441
NM_020975.6:c.43_45del