Canonical Allele Identifier: PA2826630161
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2609841
ClinVar RCV Id: RCV003364334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly158Cys
CA346744970
NM_001281493.2:c.472G>T