Canonical Allele Identifier: PA2826636162
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp501Gly
CA010206
NM_001281494.2:c.1502A>G