Canonical Allele Identifier: PA645378846
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410512
ClinVar RCV Id: RCV000562563 RCV000476123 RCV000587170 RCV001824790 RCV004001853 RCV003463941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg248Pro
CA073426
NM_000179.3:c.743G>C