Canonical Allele Identifier: PA645416577
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 264608
ClinVar RCV Id: RCV000251778 RCV000552105 RCV001529965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp955Asn
CA10587773
NM_000257.4:c.2863G>A