Canonical Allele Identifier: PA190180
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184831
ClinVar RCV Id: RCV000164156 RCV000478111 RCV000693101 RCV003995320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser860Phe
CA010453
NM_000179.3:c.2579C>T