Canonical Allele Identifier: PA2827664645
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 235532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Glu331Asp
CA10581345
NM_001352607.2:c.993G>T
CA388695105
NM_001352607.2:c.993G>C