Canonical Allele Identifier: PA2825112800
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2105624
ClinVar RCV Id: RCV003023550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1451Thr
CA389039982
NM_000257.4:c.4352A>C