Canonical Allele Identifier: PA2827664605
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Met290Arg
CA388694737
NM_001352607.2:c.869T>G