Canonical Allele Identifier: PA658680805
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483836
ClinVar RCV Id: RCV000569677 RCV001221676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser677Asn
CA346750720
NM_000179.3:c.2030G>A