Canonical Allele Identifier: PA2829942669
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 372080
ClinVar RCV Id: RCV000410987 RCV000412050 RCV000474558 RCV000574881 RCV003235199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Leu1048Val
CA042766
NM_020630.6:c.3142C>G