Canonical Allele Identifier: PA2829941632
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241341
ClinVar RCV Id: RCV000226795 RCV000410332 RCV000409197 RCV000679725 RCV001013684 RCV003469160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Ala639Thr
CA036557
NM_020630.6:c.1915G>A