Canonical Allele Identifier: PA2826636176
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133600
ClinVar RCV Id: RCV003064079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser504Ala
CA346754002
NM_001281494.2:c.1510T>G