Canonical Allele Identifier: PA645434963
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 235532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Glu357Asp
CA10581345
NM_000282.4:c.1071G>T
CA388695105
NM_000282.4:c.1071G>C