Canonical Allele Identifier: PA130243
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 38594
ClinVar RCV Id: RCV000570795 RCV000709106 RCV001046577 RCV001262456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr338Ile
CA007399
NM_020975.6:c.1013C>T