Allele Registry

Canonical Allele Identifier: PA2828048131

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014921

ClinVar Variation:

13907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Ser511Pro	CA008632 NM_001355216.1:c.1531T>C