Canonical Allele Identifier: PA128127
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24887
ClinVar RCV Id: RCV000411509 RCV000409959 RCV000465806 RCV000573056 RCV001102551 RCV001102550 RCV001107801 RCV001107802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly533Ser
CA007667
NM_020630.6:c.1597G>A