Canonical Allele Identifier: PA107207
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13907
ClinVar RCV Id: RCV000014921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser765Pro
CA008632
NM_020975.6:c.2293T>C