Canonical Allele Identifier: PA1139741067
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 941689
ClinVar RCV Id: RCV001211530 RCV002319675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.His103Tyr
CA376770535
NM_020975.6:c.307C>T