Canonical Allele Identifier: PA2828048227
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13935
ClinVar Variation Id: 38612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Leu536Phe
CA008702
NM_001355216.1:c.1608G>C
CA008709
NM_001355216.1:c.1608G>T