Canonical Allele Identifier: PA2573165172
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442807
ClinVar RCV Id: RCV001960363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1577Ser
CA389037767
NM_000257.4:c.4729G>T