Canonical Allele Identifier: PA169459
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89228
ClinVar RCV Id: RCV000132230 RCV000221704 RCV000524122 RCV003460665 RCV003997069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu619Asp
CA009330
NM_000179.3:c.1857A>C
CA346749794
NM_000179.3:c.1857A>T