Canonical Allele Identifier: PA2826631681
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491944
ClinVar RCV Id: RCV002010196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys512Asn
CA346754053
NM_001281493.2:c.1536G>C
CA346754054
NM_001281493.2:c.1536G>T