Canonical Allele Identifier: PA2827665912
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1936460
ClinVar RCV Id: RCV002658022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339539.1:p.Leu67Arg
CA388695263
NM_001352610.2:c.200T>G