Canonical Allele Identifier: PA2499230268
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284717
ClinVar RCV Id: RCV001699870 RCV001882775 RCV003150454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1092Thr
CA036593
NM_000257.4:c.3274G>A