Canonical Allele Identifier: PA2827663928
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 310845
ClinVar RCV Id: RCV000282575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Ile260Leu
CA7033379
NM_001352606.2:c.778A>C
CA388694337
NM_001352606.2:c.778A>T