Canonical Allele Identifier: PA2826627222
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 922475
ClinVar RCV Id: RCV001182585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala657Ser
CA346753602
NM_001281492.2:c.1969G>T