Canonical Allele Identifier: PA2827666657
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 429410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Ser157Cys
CA7033719
NM_001352612.2:c.469A>T