Canonical Allele Identifier: PA2827664901
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218253
ClinVar RCV Id: RCV000236842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Cys615Arg
CA7033896
NM_001352607.2:c.1843T>C