Canonical Allele Identifier: PA2826630101
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_001268422.1:p.Ser143Arg
CA346744540
NM_001281493.2:c.427A>C
CA346744554
NM_001281493.2:c.429T>A
CA346744555
NM_001281493.2:c.429T>G