Canonical Allele Identifier: PA1139671765
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 956719
ClinVar RCV Id: RCV001229578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys234Glu
CA389052230
NM_000257.4:c.700A>G