Canonical Allele Identifier: PA169374
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142773
ClinVar RCV Id: RCV000132174 RCV000541079 RCV001267890 RCV001174713 RCV002514752 RCV003462035
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1157Cys
CA012982
NM_000179.3:c.3469G>T