Canonical Allele Identifier: PA658681441
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn1273Lys
CA072193
NM_000179.3:c.3819T>G
CA346761246
NM_000179.3:c.3819T>A