Canonical Allele Identifier: PA2827665174
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 449078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Lys272Arg
CA388694612
NM_001352608.2:c.815A>G