Canonical Allele Identifier: PA2825139103
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 3023607
ClinVar RCV Id: RCV003880702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Val321Ala
CA388694769
NM_000282.4:c.962T>C