Canonical Allele Identifier: PA2825089659
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791169
ClinVar RCV Id: RCV002450458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu810Asp
CA346754028
NM_000179.3:c.2430G>T
CA346754029
NM_000179.3:c.2430G>C