Canonical Allele Identifier: PA2827664610
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1803092
ClinVar RCV Id: RCV002466762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339536.1:p.Ala294Asp
CA388694762
NM_001352607.2:c.881C>A