Canonical Allele Identifier: PA2826634312
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823498
ClinVar RCV Id: RCV001019792 RCV001860958
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser26Gly
CA346741038
NM_001281494.2:c.76A>G