Canonical Allele Identifier: PA2828048187
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2625015
ClinVar RCV Id: RCV003377694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Asn523Lys
CA376555699
NM_001355216.1:c.1569C>A
CA376555701
NM_001355216.1:c.1569C>G