Canonical Allele Identifier: PA161939
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135183
ClinVar RCV Id: RCV000121987 RCV000554385 RCV000567241 RCV002483229 RCV004528836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asp102Asn
CA009176
NM_020975.6:c.304G>A