Canonical Allele Identifier: PA2826630804
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479872
ClinVar Variation Id: 953393
ClinVar RCV Id: RCV001225680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser309Arg
CA346749544
NM_001281493.2:c.925A>C
CA346749562
NM_001281493.2:c.927T>G
CA346749565
NM_001281493.2:c.927T>A