Canonical Allele Identifier: PA2828048753
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216721
ClinVar RCV Id: RCV000196286 RCV002478713 RCV002433890 RCV003441780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.His672Asp
CA040885
NM_001355216.1:c.2014C>G