Canonical Allele Identifier: PA2827664653
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2039433
ClinVar RCV Id: RCV002899889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Leu343Val
CA7033510
NM_001352607.2:c.1027C>G