Canonical Allele Identifier: PA658680829
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 486904
ClinVar RCV Id: RCV000570696
ClinVar Variation Id: 1785817
ClinVar RCV Id: RCV002424129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu699Asp
CA346750887
NM_000179.3:c.2097G>C
CA346750888
NM_000179.3:c.2097G>T