Canonical Allele Identifier: PA345340
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys1014del
CA069980
NM_000179.3:c.3040_3042del
CA346756475
NM_000179.3:c.3037A>T
CA346756482
NM_000179.3:c.3040A>T