Canonical Allele Identifier: PA2828434351
Gene: ABCC11 HGNC NCBI

Linked Data

ClinVar Variation Id: 779015
ClinVar RCV Id: RCV000959760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357425.1:p.Val491Ile
CA8043868
NM_001370496.1:c.1471G>A