Canonical Allele Identifier: PA2826636505
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525617
ClinVar RCV Id: RCV000629726 RCV002457983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys583Asn
CA346755177
NM_001281494.2:c.1749A>C
CA346755178
NM_001281494.2:c.1749A>T