Canonical Allele Identifier: PA2826636437
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479929
ClinVar RCV Id: RCV000570721 RCV000588628 RCV000692110 RCV001821659 RCV003459291 RCV004000882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met566Ile
CA069280
NM_001281494.2:c.1698G>A
CA346754948
NM_001281494.2:c.1698G>C
CA346754949
NM_001281494.2:c.1698G>T