Canonical Allele Identifier: PA2826637340
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro775Gln
CA10578134
NM_001281494.2:c.2324C>A