Canonical Allele Identifier: PA2827665914
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1426554
ClinVar RCV Id: RCV001933417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339539.1:p.Lys70Arg
CA7033518
NM_001352610.2:c.209A>G