Canonical Allele Identifier: CA2336487497

Gene: PCAT19

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41479679G= , CM000681.2:g.41479679G=	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
NR_040109.1:n.950-395C=
NR_040109.2:n.955-395C=
NR_136334.1:n.67-395C=