Canonical Allele Identifier: CA913171838
Gene:

Linked Data

ClinVar Variation Id: 690206
ClinVar RCV Id: RCV000851096
dbSNP Id: rs1556424481
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14696A>C , J01415.2:m.14696A>C GRCh38
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