Canonical Allele Identifier: PA2580441369
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2166006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Phe612Leu
CA376552771
NM_020975.6:c.1834T>C
CA376552776
NM_020975.6:c.1836C>A
CA376552777
NM_020975.6:c.1836C>G