Canonical Allele Identifier: PA645511184
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1081Trp
CA346758098
NM_000179.3:c.3242T>G