Canonical Allele Identifier: CA327608135
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs762682503

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082302del , CM000685.2:g.23082302del GRCh38
NC_000023.10:g.23100419del , CM000685.1:g.23100419del GRCh37
NC_000023.9:g.23010340del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18180del
NR_073010.2:n.260-18180del