Canonical Allele Identifier: PA161924
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135181
ClinVar RCV Id: RCV000121983 RCV000409698 RCV000532140 RCV000412388 RCV001577914 RCV002321601 RCV003460860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Tyr1062Cys
CA009211
NM_020630.6:c.3185A>G