Canonical Allele Identifier: PA2827609508
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 559329
ClinVar RCV Id: RCV000676893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338360.1:p.Phe129Leu
CA195893154
NM_001351431.2:c.385T>C
CA373835261
NM_001351431.2:c.387C>G
CA373835262
NM_001351431.2:c.387C>A