Canonical Allele Identifier: PA915963634
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 652505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met303Leu
CA46706955
NM_000179.3:c.907A>T
CA346740711
NM_000179.3:c.907A>C