Canonical Allele Identifier: PA915965008
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_000170.1:p.Lys771Asn
CA346753147
NM_000179.3:c.2313G>C
CA346753156
NM_000179.3:c.2313G>T