Canonical Allele Identifier: PA1139766714
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 922063
ClinVar Variation Id: 924740
ClinVar RCV Id: RCV001186286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777596.2:p.Leu21_Leu23del
CA417957276
NM_174936.4:c.57_65del
CA913187506
NM_174936.4:c.42_50del