Canonical Allele Identifier: PA2827665202
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 495792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Met290Lys
CA388694736
NM_001352608.2:c.869T>A