Canonical Allele Identifier: PA658805345
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 543729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro20Ser
CA376768100
NM_020975.6:c.58C>T