Canonical Allele Identifier: PA123638
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13955
ClinVar RCV Id: RCV000014983 RCV000206045 RCV000562190 RCV001105834 RCV001105833 RCV001108067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val778Ile
CA008677
NM_020975.6:c.2332G>A