Canonical Allele Identifier: CA913177921

Gene:

Linked Data

• ClinVar Variation Id: 689897
• ClinVar RCV Id: RCV000850748
• dbSNP Id: rs1603219433

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4375C>T , J01415.2:m.4375C>T	GRCh38