Canonical Allele Identifier: PA2828705748
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775942
ClinVar RCV Id: RCV002398459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Thr243Ser
CA233633317
NM_001377274.1:c.728C>G
CA384139040
NM_001377274.1:c.727A>T