Canonical Allele Identifier: PA2827665702
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2130507
ClinVar RCV Id: RCV003052115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Val376Ala
CA388695227
NM_001352609.2:c.1127T>C