Canonical Allele Identifier: PA2826637388
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127584
ClinVar RCV Id: RCV000115410 RCV000121584 RCV000168382 RCV000589544 RCV001787917 RCV003997248 RCV004528800 RCV001808341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785His
CA012253
NM_001281494.2:c.2354C>A