Canonical Allele Identifier: PA2826633689
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met965Ile
CA346761198
NM_001281493.2:c.2895G>C
CA346761199
NM_001281493.2:c.2895G>T
CA346761200
NM_001281493.2:c.2895G>A