Canonical Allele Identifier: PA2827665001
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218248
ClinVar RCV Id: RCV000235343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Asp69Gly
CA10575823
NM_001352608.2:c.206A>G