Canonical Allele Identifier: PA2827666793
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Gly305Arg
CA7033866
NM_001352612.2:c.913G>A
CA388640367
NM_001352612.2:c.913G>C