Canonical Allele Identifier: PA2827665479
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Gly594Arg
CA7033866
NM_001352608.2:c.1780G>A
CA388640367
NM_001352608.2:c.1780G>C