Canonical Allele Identifier: PA2825091178
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 660233
ClinVar RCV Id: RCV002325607 RCV000817387
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1116Ser
CA346758747
NM_000179.3:c.3346G>A