Canonical Allele Identifier: PA129700
Gene: ASCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 31129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185727.1:p.Asn290Ser
CA129699
NM_001198798.2:c.869A>G