Canonical Allele Identifier: PA2826632834
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro780Gln
CA346758111
NM_001281493.2:c.2339C>A