Canonical Allele Identifier: PA2825653942
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_001121164.1:p.Val295Ala
CA388694769
NM_001127692.3:c.884T>C