Canonical Allele Identifier: PA2829939690
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 405549
ClinVar RCV Id: RCV000473800 RCV001294033 RCV002348280 RCV003322771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg177Gln
CA043905
NM_020630.6:c.530G>A