Canonical Allele Identifier: PA2826634296
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230518
ClinVar RCV Id: RCV000216324 RCV000229706 RCV000483787 RCV000663012 RCV001328357 RCV003462441 RCV003997842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys22Asn
CA10578055
NM_001281494.2:c.66A>C
CA346740965
NM_001281494.2:c.66A>T