Canonical Allele Identifier: PA161942
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13947
ClinVar RCV Id: RCV000014974 RCV000121988 RCV000198261 RCV000163885 RCV000490359 RCV000755684 RCV001106779 RCV001106778 RCV001107412 RCV003389668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg114His
CA009235
NM_020630.6:c.341G>A