Canonical Allele Identifier: PA2825654022
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 662772
ClinVar RCV Id: RCV000820501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Arg373Trp
CA388695371
NM_001127692.3:c.1117C>T