Canonical Allele Identifier: PA916035568
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218258
ClinVar RCV Id: RCV000236220 RCV000611609 RCV003401094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Trp559Leu
CA7033745
NM_001352609.2:c.1676G>T