Canonical Allele Identifier: PA2826715327
Gene: RERGL HGNC NCBI

Linked Data

ClinVar Variation Id: 161770
ClinVar RCV Id: RCV000149306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273130.1:p.Gln138Lys
CA174752
NM_001286201.2:c.412C>A