Canonical Allele Identifier: PA2580441455
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2082971
ClinVar RCV Id: RCV002999546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro766Gln
CA376555563
NM_020975.6:c.2297C>A