Canonical Allele Identifier: PA2825089924
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567455
ClinVar RCV Id: RCV003311251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met875Ile
CA346755045
NM_000179.3:c.2625G>A
CA346755047
NM_000179.3:c.2625G>C
CA346755049
NM_000179.3:c.2625G>T