Canonical Allele Identifier: PA2573163641
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu773Phe
CA346753179
NM_000179.3:c.2317C>T