Canonical Allele Identifier: PA2826636380
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237160
ClinVar RCV Id: RCV001372750
ClinVar Variation Id: 336443
ClinVar RCV Id: RCV000276074 RCV000630372 RCV002256216 RCV003463784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys552Asn
CA069186
NM_001281494.2:c.1656G>T
CA10582064
NM_001281494.2:c.1656G>C