Canonical Allele Identifier: PA2826628573
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062452
ClinVar RCV Id: RCV001372169
ClinVar Variation Id: 1517382
ClinVar RCV Id: RCV002027315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1054Ile
CA346760270
NM_001281492.2:c.3162G>A
CA346760271
NM_001281492.2:c.3162G>C
CA346760272
NM_001281492.2:c.3162G>T