Canonical Allele Identifier: PA2825092269
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803163
ClinVar RCV Id: RCV002466833 RCV003594306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1255Val
CA346761112
NM_000179.3:c.3764A>T