Canonical Allele Identifier: PA188328
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136103
ClinVar RCV Id: RCV000163453 RCV000455280 RCV000727068 RCV001104479 RCV001107242 RCV001107243 RCV001104478 RCV004542931 RCV001081705 RCV002272134 RCV003153409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asp567Asn
CA007711
NM_020975.6:c.1699G>A