Canonical Allele Identifier: PA658829698
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 559329
ClinVar RCV Id: RCV000676893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001689.1:p.Phe238Leu
CA195893154
NM_001698.3:c.712T>C
CA373835261
NM_001698.3:c.714C>G
CA373835262
NM_001698.3:c.714C>A