Canonical Allele Identifier: PA913193979
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 626823
ClinVar RCV Id: RCV000770504 RCV002533965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg54Leu
CA028998
NM_000257.4:c.161G>T