Canonical Allele Identifier: PA129701
Gene: ASCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 31129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185728.1:p.Asn318Ser
CA129699
NM_001198799.3:c.953A>G