Canonical Allele Identifier: PA2825091030
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 654260
ClinVar RCV Id: RCV000810186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys1092Asn
CA346758280
NM_000179.3:c.3276A>C
CA346758284
NM_000179.3:c.3276A>T