Canonical Allele Identifier: PA2826915452
Gene: AUH HGNC NCBI

Linked Data

ClinVar Variation Id: 1502193
ClinVar RCV Id: RCV002020116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293119.1:p.Met201Ile
CA373835313
NM_001306190.2:c.603G>C
CA373835314
NM_001306190.2:c.603G>A
CA373835315
NM_001306190.2:c.603G>T