Canonical Allele Identifier: PA2827663373
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 235532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Glu357Asp
CA10581345
NM_001352605.2:c.1071G>T
CA388695105
NM_001352605.2:c.1071G>C