Allele Registry

Canonical Allele Identifier: PA2828705907

Gene: ABCC9 HGNC NCBI

ClinVar RCV:

RCV000029274

RCV000038600

RCV000172738

RCV000251925

RCV000852670

RCV001082826

RCV001528354

ClinVar Variation:

35627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364203.1:p.Val446Ile	CA199985 NM_001377274.1:c.1336G>A