Canonical Allele Identifier: PA645391696
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89369
ClinVar RCV Id: RCV000074836 RCV000218926 RCV000223174 RCV000587747 RCV000524169 RCV000764431 RCV001358521 RCV003460680 RCV004019095 RCV004542742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr970Met
CA012473
NM_001281492.2:c.2909C>T