Canonical Allele Identifier: PA2826634036
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410496
ClinVar RCV Id: RCV000571258 RCV000473620 RCV004001847 RCV002307506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asn1025Tyr
CA16611088
NM_001281493.2:c.3073A>T