Canonical Allele Identifier: PA357594
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220159
ClinVar RCV Id: RCV000205628 RCV000481950 RCV000562735 RCV000662811 RCV002247633 RCV003997619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser1279Asn
CA349759
NM_000179.3:c.3836G>A