Canonical Allele Identifier: PA346512
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 180435
ClinVar RCV Id: RCV000157355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn444Thr
CA010577
NM_000257.4:c.1331A>C