Canonical Allele Identifier: PA123168
Gene: PIGR HGNC NCBI

Linked Data

ClinVar Variation Id: 13526
ClinVar RCV Id: RCV000014481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002635.2:p.Ala580Val
CA123167
NM_002644.4:c.1739C>T