Canonical Allele Identifier: PA2828705835
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 240202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Thr371Ala
CA10583040
NM_001377274.1:c.1111A>G