Canonical Allele Identifier: CA913168996
Gene:
ClinVar Allele:
677695
ClinVar RCV:
RCV000850693
ClinVar Variation:
689858
dbSNP:
199474661
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3252A>T , J01415.2:m.3252A>T GRCh38
Search 100 bp 5'
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