Canonical Allele Identifier: PA2828047602
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24913
ClinVar RCV Id: RCV000519407 RCV000696792 RCV000564566 RCV001818172 RCV003460488 RCV002477000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asp377Asn
CA008190
NM_001355216.1:c.1129G>A