Canonical Allele Identifier: PA2825112174
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072044
ClinVar RCV Id: RCV004012074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1053Leu
CA389045348
NM_000257.4:c.3158G>T