Canonical Allele Identifier: PA2827665001
Gene: PCCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Asp69Gly
CA10575823
NM_001352608.2:c.206A>G