Canonical Allele Identifier: PA2827666493
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.Gly335Arg
CA7033866
NM_001352611.2:c.1003G>A
CA388640367
NM_001352611.2:c.1003G>C