Canonical Allele Identifier: PA2826629151
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736032
ClinVar RCV Id: RCV002373095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1171Ile
CA346761426
NM_001281492.2:c.3512A>T