Canonical Allele Identifier: PA915957096
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 636549
ClinVar RCV Id: RCV000788407 RCV001110336 RCV001177782 RCV001110337 RCV001306143 RCV002440621 RCV003320212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met922Thr
CA034223
NM_000257.4:c.2765T>C