Canonical Allele Identifier: PA2826625140
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 962527
ClinVar RCV Id: RCV001236401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys171Asn
CA346740705
NM_001281492.2:c.513G>C
CA346740706
NM_001281492.2:c.513G>T