Canonical Allele Identifier: PA2826631011
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479971
ClinVar Variation Id: 2837716
ClinVar RCV Id: RCV003758378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln355His
CA346750604
NM_001281493.2:c.1065G>C
CA346750605
NM_001281493.2:c.1065G>T