Canonical Allele Identifier: PA2826631329
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483778
ClinVar RCV Id: RCV000575588 RCV000706558 RCV004001050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala427Val
CA346751247
NM_001281493.2:c.1280C>T