Canonical Allele Identifier: PA2826629615
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483814
ClinVar RCV Id: RCV000566160 RCV001055886 RCV003332204 RCV004001058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser28Pro
CA073692
NM_001281493.2:c.82T>C