Canonical Allele Identifier: PA2826631031
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 998688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met360Leu
CA346750631
NM_001281493.2:c.1078A>C
CA346750632
NM_001281493.2:c.1078A>T