Canonical Allele Identifier: PA2827665304
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Ile401Val
CA145988
NM_001352608.2:c.1201A>G