Canonical Allele Identifier: PA645441455
Gene: INHA HGNC NCBI

Linked Data

ClinVar Variation Id: 402979
ClinVar RCV Id: RCV000456099 RCV001258300 RCV003912792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002182.1:p.Ala257Thr
CA2132051
NM_002191.4:c.769G>A