Canonical Allele Identifier: PA645381798
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233251
ClinVar RCV Id: RCV000217257 RCV002515705 RCV003462520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr754Ser
CA10578103
NM_000179.3:c.2260A>T
CA346752762
NM_000179.3:c.2261C>G