Canonical Allele Identifier: PA332911
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136108
ClinVar RCV Id: RCV000123307 RCV000562548 RCV003492551 RCV002483239 RCV003159099 RCV003467095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Lys722Asn
CA008592
NM_020975.6:c.2166G>T
CA376554271
NM_020975.6:c.2166G>C