Canonical Allele Identifier: PA2826636740
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232656
ClinVar RCV Id: RCV000220173 RCV003765429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp634Asn
CA10578119
NM_001281494.2:c.1900G>A