Canonical Allele Identifier: PA645381495
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237151
ClinVar RCV Id: RCV000227011 RCV000483631 RCV000580465 RCV000662419 RCV003469132 RCV003998715
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met703Val
CA068470
NM_000179.3:c.2107A>G