Canonical Allele Identifier: PA2827666682
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Val188Phe
CA292687
NM_001352612.2:c.562G>T