Canonical Allele Identifier: PA2828048553
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 3227534
ClinVar RCV Id: RCV004524652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gln606His
CA376556711
NM_001355216.1:c.1818G>C
CA376556716
NM_001355216.1:c.1818G>T