Canonical Allele Identifier: PA098981
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14122
ClinVar RCV Id: RCV000192200 RCV000777877 RCV000989191 RCV000767122 RCV001087154 RCV002496367 RCV000035714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr441Met
CA010543
NM_000257.4:c.1322C>T