Canonical Allele Identifier: PA107281
Gene: PCCA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Ala138Thr
CA343123
NM_000282.4:c.412G>A