Canonical Allele Identifier: PA2827666801
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Val310Leu
CA7033870
NM_001352612.2:c.928G>C