Canonical Allele Identifier: PA356919
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 219872
ClinVar RCV Id: RCV000206643 RCV000561732 RCV002494521 RCV002285278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg418Gln
CA032301
NM_020975.6:c.1253G>A