Canonical Allele Identifier: PA337725
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216722
ClinVar RCV Id: RCV000198200 RCV000662775 RCV000679738 RCV001017530 RCV003462337 RCV002492921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser977Arg
CA041466
NM_020975.6:c.2931C>G
CA376557985
NM_020975.6:c.2929A>C
CA376557989
NM_020975.6:c.2931C>A