Canonical Allele Identifier: PA658802238
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525805
ClinVar RCV Id: RCV000630124
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro768Arg
CA46710789
NM_000179.3:c.2303C>G