Canonical Allele Identifier: PA2826625756
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 648188
ClinVar RCV Id: RCV000802856 RCV002386433 RCV004001653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser315Arg
CA346744540
NM_001281492.2:c.943A>C
CA346744554
NM_001281492.2:c.945T>A
CA346744555
NM_001281492.2:c.945T>G