Canonical Allele Identifier: PA1139674525
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 936576
ClinVar RCV Id: RCV001205404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys692Asn
CA346750807
NM_000179.3:c.2076A>C
CA346750808
NM_000179.3:c.2076A>T