Canonical Allele Identifier: PA1139671766
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 928852
ClinVar RCV Id: RCV001193368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr235Asn
CA389052220
NM_000257.4:c.704C>A