Canonical Allele Identifier: PA2827665485
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 459937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Val599Leu
CA7033870
NM_001352608.2:c.1795G>C