Canonical Allele Identifier: PA349463
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 219791
ClinVar RCV Id: RCV000205293 RCV002399761 RCV003153481 RCV003462370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Val351Glu
CA030932
NM_020630.6:c.1052T>A