Canonical Allele Identifier: PA645383970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1148Ser
CA070946
NM_000179.3:c.3442G>A