Canonical Allele Identifier: PA2580209589
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_001339540.1:p.Leu54Val
CA7033510
NM_001352611.2:c.160C>G