Canonical Allele Identifier: PA658681273
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483844
ClinVar RCV Id: RCV000571300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1084Asn
CA346758119
NM_000179.3:c.3250G>A