Canonical Allele Identifier: PA1139674719
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 948777
ClinVar RCV Id: RCV001220101 RCV002418756 RCV003462747
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn748Ser
CA346752616
NM_000179.3:c.2243A>G