Canonical Allele Identifier: PA2826636029
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 665100
ClinVar RCV Id: RCV000823311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys469Asn
CA346753147
NM_001281494.2:c.1407G>C
CA346753156
NM_001281494.2:c.1407G>T