Canonical Allele Identifier: PA2499229390
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023446
ClinVar RCV Id: RCV001323487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met654Ile
CA068329
NM_000179.3:c.1962G>A
CA346750584
NM_000179.3:c.1962G>C
CA346750585
NM_000179.3:c.1962G>T