Canonical Allele Identifier: PA658744114
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490020
ClinVar RCV Id: RCV000581061 RCV000797264 RCV001284187 RCV001779017 RCV003459433 RCV004001272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys145Asn
CA346737166
NM_000179.3:c.435A>C
CA346737167
NM_000179.3:c.435A>T