Canonical Allele Identifier: PA2829938990
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2713355
ClinVar RCV Id: RCV003534112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly10Arg
CA376768048
NM_020630.6:c.28G>A
CA376768049
NM_020630.6:c.28G>C