Canonical Allele Identifier: PA330359
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89188
ClinVar RCV Id: RCV000074650
ClinVar Variation Id: 2859099
ClinVar RCV Id: RCV003759249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu446Asp
CA008501
NM_000179.3:c.1338A>T
CA346744577
NM_000179.3:c.1338A>C