Canonical Allele Identifier: PA658670383
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486314
ClinVar RCV Id: RCV000567474 RCV000802145 RCV002476249 RCV003225093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg368Cys
CA031579
NM_020975.6:c.1102C>T