Canonical Allele Identifier: PA2828048903
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216722
ClinVar RCV Id: RCV000198200 RCV000662775 RCV000679738 RCV001017530 RCV003462337 RCV002492921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ser723Arg
CA041466
NM_001355216.1:c.2169C>G
CA376557985
NM_001355216.1:c.2167A>C
CA376557989
NM_001355216.1:c.2169C>A