Canonical Allele Identifier: PA2825088742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2693765
ClinVar RCV Id: RCV003594731 RCV004364920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly599Glu
CA346749319
NM_000179.3:c.1796G>A