Canonical Allele Identifier: PA2828048186
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asn523Ser
CA008672
NM_001355216.1:c.1568A>G