Canonical Allele Identifier: CA913163370
Gene:

Linked Data

ClinVar Variation Id: 689846
ClinVar RCV Id: RCV000850677 RCV001796793
dbSNP Id: rs587776441
ERepo: CA913163370/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1644G>A , J01415.2:m.1644G>A GRCh38
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