Canonical Allele Identifier: PA190022
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184777
ClinVar RCV Id: RCV000164092 RCV000808381 RCV003462125 RCV003313045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser24Leu
CA016332
NM_000179.3:c.71C>T