Canonical Allele Identifier: PA2829941952
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1789288
ClinVar RCV Id: RCV002446328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ser767Asn
CA376555577
NM_020630.6:c.2300G>A