Canonical Allele Identifier: PA2573274620
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1481838
ClinVar RCV Id: RCV002442988 RCV002025033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser819Arg
CA376556228
NM_020975.6:c.2455A>C
CA376556240
NM_020975.6:c.2457C>A
CA376556242
NM_020975.6:c.2457C>G