Canonical Allele Identifier: PA2825088995
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073290
ClinVar RCV Id: RCV004015304
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser648Gly
CA46709970
NM_000179.3:c.1942A>G