Canonical Allele Identifier: PA2825088732
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780101
ClinVar Variation Id: 1780131
ClinVar RCV Id: RCV002407740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe596Leu
CA346749264
NM_000179.3:c.1786T>C
CA346749275
NM_000179.3:c.1788T>A
CA346749276
NM_000179.3:c.1788T>G