Canonical Allele Identifier: PA658680138
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455252
ClinVar RCV Id: RCV000537161 RCV000575269 RCV000781599 RCV004003690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn112Lys
CA346736957
NM_000179.3:c.336C>G
CA346736958
NM_000179.3:c.336C>A