Canonical Allele Identifier: PA2825089393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2826467
ClinVar RCV Id: RCV003761094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn751Lys
CA346752676
NM_000179.3:c.2253T>A
CA346752688
NM_000179.3:c.2253T>G