Canonical Allele Identifier: PA1139674925
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 956885
ClinVar RCV Id: RCV001229769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1549Gly
CA389037940
NM_000257.4:c.4646C>G