Canonical Allele Identifier: PA2573163507
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu699Lys
CA346750877
NM_000179.3:c.2095G>A