Canonical Allele Identifier: PA2827664278
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Val625Leu
CA7033870
NM_001352606.2:c.1873G>C