Canonical Allele Identifier: PA2826915454
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 559329
ClinVar RCV Id: RCV000676893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Phe209Leu
CA195893154
NM_001306190.2:c.625T>C
CA373835261
NM_001306190.2:c.627C>G
CA373835262
NM_001306190.2:c.627C>A