Canonical Allele Identifier: PA169917
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys854del
CA010414
NM_000179.3:c.2561_2563del
CA346754593
NM_000179.3:c.2554A>T
CA346754630
NM_000179.3:c.2557A>T
CA346754650
NM_000179.3:c.2560A>T