Canonical Allele Identifier: PA2827665293
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 882229
ClinVar RCV Id: RCV001111728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Asp394Glu
CA7033640
NM_001352608.2:c.1182T>G
CA388695849
NM_001352608.2:c.1182T>A