Canonical Allele Identifier: PA128385
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24945
ClinVar RCV Id: RCV000478761 RCV000529442 RCV000567481 RCV000662806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg833Cys
CA008813
NM_020630.6:c.2497C>T