Canonical Allele Identifier: PA2826915451
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 3132330
ClinVar RCV Id: RCV004421258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Gly200Arg
CA373835325
NM_001306190.2:c.598G>C
CA373835326
NM_001306190.2:c.598G>A