Canonical Allele Identifier: PA1139673994
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 954641
ClinVar RCV Id: RCV001227137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1174Leu
CA389043610
NM_000257.4:c.3520A>C
CA389043611
NM_000257.4:c.3520A>T