Canonical Allele Identifier: PA2825801014
Gene: LRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2215480
ClinVar RCV Id: RCV002656315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129175.1:p.Thr189Ala
CA4839077
NM_001135703.3:c.565A>G