Canonical Allele Identifier: PA645381881
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro768Ala
CA068796
NM_000179.3:c.2302C>G