Canonical Allele Identifier: PA2825111942
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795994
ClinVar RCV Id: RCV002441368 RCV003238896 RCV003586374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu929Asp
CA034324
NM_000257.4:c.2787G>C
CA389047058
NM_000257.4:c.2787G>T