Canonical Allele Identifier: CA508216409

Gene: PPIAP59

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50927340A>T , CM000681.2:g.50927340A>T	GRCh38
NC_000019.9:g.51430596A>T , CM000681.1:g.51430596A>T	GRCh37
NC_000019.8:g.56122408A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000596021.1:n.232T>A