Canonical Allele Identifier: PA1139675248
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 976304
ClinVar RCV Id: RCV003320243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1660Pro
CA389037205
NM_000257.4:c.4978G>C