Canonical Allele Identifier: PA2826626276
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485855
ClinVar RCV Id: RCV000575004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile440Leu
CA346748557
NM_001281492.2:c.1318A>C
CA346748563
NM_001281492.2:c.1318A>T