Canonical Allele Identifier: PA2828046950
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241336
ClinVar RCV Id: RCV000234316 RCV001011698 RCV001107800 RCV001107138 RCV000709111 RCV001107139 RCV001770206 RCV001107140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Thr234Ser
CA033750
NM_001355216.1:c.700A>T
CA376549755
NM_001355216.1:c.701C>G