Canonical Allele Identifier: PA658804495
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 519168
ClinVar RCV Id: RCV000620051 RCV002531765 RCV004002672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1149Pro
CA389043860
NM_000257.4:c.3446G>C