Canonical Allele Identifier: PA915964750
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644624
ClinVar RCV Id: RCV000798582
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu675Gly
CA346750707
NM_000179.3:c.2024A>G