Canonical Allele Identifier: PA2825087159
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101336
ClinVar RCV Id: RCV003016854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu288Asp
CA346740607
NM_000179.3:c.864A>C
CA346740608
NM_000179.3:c.864A>T