Canonical Allele Identifier: PA188357
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136115
ClinVar RCV Id: RCV000163463 RCV000679744 RCV000663277 RCV000761007 RCV001106024 RCV001108239 RCV001083486 RCV001106025 RCV001818296 RCV004528841 RCV001108238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr1038Ala
CA009187
NM_020975.6:c.3112A>G