Canonical Allele Identifier: PA2826629163
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738992
ClinVar RCV Id: RCV003593443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1172Val
CA346761434
NM_001281492.2:c.3515C>T