Canonical Allele Identifier: CA861404963
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1167907153

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120428del , CM000671.2:g.15120428del GRCh38
NC_000009.11:g.15120426del , CM000671.1:g.15120426del GRCh37
NC_000009.10:g.15110426del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5302del