Canonical Allele Identifier: PA2825653997
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2069132
ClinVar RCV Id: RCV002958757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.His358Gln
CA255987364
NM_001127692.3:c.1074C>A
CA388695278
NM_001127692.3:c.1074C>G