Canonical Allele Identifier: PA658750805
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495720
ClinVar RCV Id: RCV000589495 RCV000818032 RCV000774619 RCV004530640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1345Ile
CA072821
NM_000179.3:c.4033G>A