Canonical Allele Identifier: PA107383
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218266
ClinVar RCV Id: RCV000235940 RCV003884401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Gly668Arg
CA7033866
NM_000282.4:c.2002G>A
CA388640367
NM_000282.4:c.2002G>C