Canonical Allele Identifier: PA2825091943
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076149
ClinVar RCV Id: RCV004018466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1206Thr
CA346760578
NM_000179.3:c.3616G>A