Canonical Allele Identifier: PA190092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184803
ClinVar RCV Id: RCV000164123 RCV000204780 RCV000479969 RCV003150013 RCV003137692 RCV003995316 RCV004528909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr327Ser
CA016745
NM_000179.3:c.980C>G
CA346741015
NM_000179.3:c.979A>T