Canonical Allele Identifier: PA236996
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 191587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Pro739Ala
CA236993
NM_005691.3:c.2215C>G