Canonical Allele Identifier: PA2827666400
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.Val236Phe
CA292687
NM_001352611.2:c.706G>T