Canonical Allele Identifier: PA357364
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro673Leu
CA348430
NM_000179.3:c.2018C>T