Canonical Allele Identifier: PA915964759
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820569
ClinVar RCV Id: RCV001014154 RCV001364767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala680Thr
CA346750737
NM_000179.3:c.2038G>A