Canonical Allele Identifier: PA1139675222
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 844103
ClinVar RCV Id: RCV001046871 RCV002451187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu811Phe
CA346754032
NM_000179.3:c.2431C>T