Canonical Allele Identifier: PA645441391
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 240202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Thr659Ala
CA10583040
NM_020297.3:c.1975A>G