Canonical Allele Identifier: PA107226
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13951
ClinVar RCV Id: RCV000014978 RCV000014979 RCV000227193 RCV000394478 RCV000431535 RCV000441854 RCV000445273 RCV000425892 RCV001016276 RCV001804732 RCV002490368 RCV003387503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser891Ala
CA008989
NM_020975.6:c.2671T>G