Canonical Allele Identifier: PA2573074282
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 369679
ClinVar RCV Id: RCV000408624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Phe5Ser
CA10654763
NM_001377274.1:c.14T>C