Canonical Allele Identifier: PA1139744326
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 973522
ClinVar RCV Id: RCV001250144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Ala775Pro
CA384118511
NM_001377274.1:c.2323G>C