Canonical Allele Identifier: PA333989
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 188078
ClinVar RCV Id: RCV000167906 RCV000409785 RCV000410975 RCV000994377 RCV001107611 RCV001107613 RCV001107612 RCV001107614 RCV002381533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Trp324Cys
CA009409
NM_020630.6:c.972G>C
CA376546185
NM_020630.6:c.972G>T