Canonical Allele Identifier: PA2827665909
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 194163
ClinVar RCV Id: RCV000174464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339539.1:p.Gly64Val
CA240005
NM_001352610.2:c.191G>T