Canonical Allele Identifier: PA356852
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 220266
ClinVar RCV Id: RCV000205988 RCV001015870
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Met848Ile
CA039702
NM_020975.6:c.2544G>A
CA376556524
NM_020975.6:c.2544G>C
CA376556525
NM_020975.6:c.2544G>T