Canonical Allele Identifier: PA2580209602
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2069132
ClinVar RCV Id: RCV002958757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.His69Gln
CA255987364
NM_001352611.2:c.207C>A
CA388695278
NM_001352611.2:c.207C>G