Canonical Allele Identifier: PA645378677
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232585
ClinVar RCV Id: RCV000223134 RCV000228836 RCV001201254 RCV001355754 RCV003462500 RCV003997984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn223Asp
CA073334
NM_000179.3:c.667A>G