Canonical Allele Identifier: PA645434992
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218253
ClinVar RCV Id: RCV000236842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Cys688Arg
CA7033896
NM_000282.4:c.2062T>C