Canonical Allele Identifier: PA2825089213
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786139
ClinVar RCV Id: RCV002417516 RCV003759710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn705Asp
CA346750949
NM_000179.3:c.2113A>G