Canonical Allele Identifier: PA2825092632
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715652
ClinVar RCV Id: RCV002304602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1302Ser
CA346761431
NM_000179.3:c.3904G>T