Canonical Allele Identifier: PA161913
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135178
ClinVar RCV Id: RCV000121980 RCV000410090 RCV000412123 RCV000724767 RCV000540063 RCV000561957 RCV003460859 RCV004530033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asn783Thr
CA008694
NM_020975.6:c.2348A>C