Canonical Allele Identifier: PA2828046730
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136098
ClinVar RCV Id: RCV000123295 RCV000572664 RCV000761174 RCV002483237 RCV002466439 RCV004530053 RCV003460874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asn194Lys
CA007539
NM_001355216.1:c.582C>G
CA376549108
NM_001355216.1:c.582C>A