Canonical Allele Identifier: PA112660
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3657
ClinVar RCV Id: RCV000003842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Met317Ile
CA116414
NM_000229.2:c.951G>A
CA396375990
NM_000229.2:c.951G>T
CA396375991
NM_000229.2:c.951G>C