Canonical Allele Identifier: CA10576203
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 225986
dbSNP Id: rs2952768

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.207629510T>C , CM000664.2:g.207629510T>C GRCh38
NC_000002.11:g.208494234T>C , CM000664.1:g.208494234T>C GRCh37
NC_000002.10:g.208202479T>C NCBI36