Canonical Allele Identifier: PA215913
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41845
ClinVar RCV Id: RCV000034777 RCV000123327 RCV000148775 RCV000223157 RCV000573525 RCV000663296 RCV001104177 RCV001103898 RCV001103896 RCV001103897 RCV001269367 RCV004528165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val262Ala
CA009350
NM_020975.6:c.785T>C