Canonical Allele Identifier: PA299509
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182656
ClinVar RCV Id: RCV000160711 RCV000217717 RCV000456306 RCV000986705 RCV000781604 RCV001030488 RCV003467255 RCV003998510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg178Cys
CA015802
NM_000179.3:c.532C>T