Canonical Allele Identifier: PA2826626807
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676789
ClinVar RCV Id: RCV003470245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe559Leu
CA346750785
NM_001281492.2:c.1675T>C
CA346750790
NM_001281492.2:c.1677C>A
CA346750791
NM_001281492.2:c.1677C>G