Canonical Allele Identifier: PA2827666499
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.Val340Leu
CA7033870
NM_001352611.2:c.1018G>C