Canonical Allele Identifier: PA123634
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13948
ClinVar RCV Id: RCV000014975 RCV000410425 RCV000148783 RCV000411688 RCV000563865 RCV000704911 RCV002490367 RCV003398513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Pro1039Leu
CA009200
NM_020630.6:c.3116C>T