Canonical Allele Identifier: CA652652066
Gene: CLCN3P1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120567T>A , CM000671.2:g.15120567T>A GRCh38
NC_000009.11:g.15120565T>A , CM000671.1:g.15120565T>A GRCh37
NC_000009.10:g.15110565T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5163A>T