Canonical Allele Identifier: PA645441962
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 228426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Pro1531Ser
CA6480809
NM_005691.3:c.4591C>T