Canonical Allele Identifier: PA196553
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187031
ClinVar RCV Id: RCV000166713 RCV000800357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg300Leu
CA016620
NM_000179.3:c.899G>T