Canonical Allele Identifier: PA658655086
Gene: C8A HGNC NCBI

Linked Data

ClinVar Variation Id: 444168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000553.1:p.Asp129Asn
CA875021
NM_000562.3:c.385G>A