Canonical Allele Identifier: PA658670252
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477335
ClinVar RCV Id: RCV000530005 RCV001013993 RCV002491104 RCV003459264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg67Cys
CA036802
NM_020975.6:c.199C>T