Canonical Allele Identifier: PA2826631361
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1787790
ClinVar RCV Id: RCV002425887
ClinVar Variation Id: 3074063
ClinVar RCV Id: RCV004012605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val436Leu
CA346752383
NM_001281493.2:c.1306G>C
CA346752385
NM_001281493.2:c.1306G>T