Canonical Allele Identifier: PA2827663641
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Gly650Arg
CA7033866
NM_001352605.2:c.1948G>A
CA388640367
NM_001352605.2:c.1948G>C