ClinGen Allele Registry
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Canonical Allele Identifier:
CA337722479
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.12925845_12925846insGA
Linked Data - NCBI & NCI
dbSNP:
16648
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12925844_12925845dup , CM000686.2:g.12925844_12925845dup
GRCh38
Search 100 bp 5'
Search 100 bp 3'