Canonical Allele Identifier: CA913180140
Gene:

Linked Data

ClinVar Variation Id: 689966
ClinVar RCV Id: RCV000850823
dbSNP Id: rs1556423019
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5655T>C , J01415.2:m.5655T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'